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Search Thermo Fisher Scientific
GCAGGCCTGCTCGGAGGGACTGCAC[A/G]CCACATCTGCCCAGCTGTTTGGCAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
HMCN2 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) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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HMCN2 - hemicentin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001291815.1 | Intron | NP_001278744.1 | ||||
XM_011518465.2 | Intron | XP_011516767.1 | ||||
XM_011518466.2 | Intron | XP_011516768.1 | ||||
XM_011518467.2 | Intron | XP_011516769.1 | ||||
XM_011518468.2 | Intron | XP_011516770.1 | ||||
XM_011518469.2 | Intron | XP_011516771.1 | ||||
XM_011518470.2 | Intron | XP_011516772.1 | ||||
XM_017014585.1 | Intron | XP_016870074.1 | ||||
XM_017014586.1 | Intron | XP_016870075.1 |