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AGAACTTTTTCATCATCGGAAACAG[A/G]AAGTGTAGCTATTAAATACTAACTC
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 160994 MIM: 613332 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
HNRNPM PubMed Links | |||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | ||||||
EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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HNRNPM - heterogeneous nuclear ribonucleoprotein M | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001297418.1 | Intron | NP_001284347.1 | ||||
NM_005968.4 | Intron | NP_005959.2 | ||||
NM_031203.3 | Intron | NP_112480.2 | ||||
XM_005272478.2 | Intron | XP_005272535.1 | ||||
XM_005272479.2 | Intron | XP_005272536.1 | ||||
XM_005272480.2 | Intron | XP_005272537.1 | ||||
XM_005272481.1 | Intron | XP_005272538.1 | ||||
XM_005272483.2 | Intron | XP_005272540.1 | ||||
XM_017026823.1 | Intron | XP_016882312.1 | ||||
XM_017026824.1 | Intron | XP_016882313.1 | ||||
XM_017026825.1 | Intron | XP_016882314.1 | ||||
XM_017026826.1 | Intron | XP_016882315.1 | ||||
XM_017026827.1 | Intron | XP_016882316.1 | ||||
XM_017026828.1 | Intron | XP_016882317.1 | ||||
XM_017026829.1 | Intron | XP_016882318.1 | ||||
XM_017026830.1 | Intron | XP_016882319.1 | ||||
XM_017026831.1 | Intron | XP_016882320.1 | ||||
XM_017026832.1 | Intron | XP_016882321.1 |
MARCH2 - membrane associated ring-CH-type finger 2 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |