Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611314 MIM: 602095 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
HMGN2P46 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 | 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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HMGN2P46 - high mobility group nucleosomal binding domain 2 pseudogene 46 | ||||||
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There are no transcripts associated with this gene. |
SLC30A4 - solute carrier family 30 member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321036.1 | 392 | Intron | NP_001307965.1 | |||
NM_013309.5 | 392 | Intron | NP_037441.2 | |||
XM_011521997.2 | 392 | UTR 5 | XP_011520299.1 | |||
XM_017022560.1 | 392 | Intron | XP_016878049.1 | |||
XM_017022561.1 | 392 | Intron | XP_016878050.1 | |||
XM_017022562.1 | 392 | Intron | XP_016878051.1 |
Set Membership: |
HapMap |