Canonical Allele Identifier: CA3710813
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs762557997
ExAC: 6:31239144 T / C
gnomAD v2: 6-31239144-T-C
gnomAD v3: 6-31271367-T-C
gnomAD v4: 6-31271367-T-C
MyVariant Identifiers: chr6:g.31239144T>C (hg19) chr6:g.31271367T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271367T>C , CM000668.2:g.31271367T>C GRCh38
NC_000006.11:g.31239144T>C , CM000668.1:g.31239144T>C GRCh37
NC_000006.10:g.31347123T>C NCBI36
NG_029422.2:g.5765A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-19A>G MANE Select ENSP00000365402.5:n.344-19A>G
ENST00000376228.9:c.344-19A>G ENSP00000365402.5:n.344-19A>G
ENST00000376237.8:c.344-36A>G ENSP00000365412.4:n.344-36A>G
ENST00000383329.7:c.344-19A>G ENSP00000372819.3:n.344-19A>G
ENST00000415537.1:c.342-19A>G
ENST00000484378.1:n.594A>G
ENST00000487245.5:n.684A>G
ENST00000495835.1:n.533-19A>G
NM_002117.5:c.344-19A>G NP_002108.4:n.344-19A>G
NM_002117.6:c.344-19A>G MANE Select NP_002108.4:n.344-19A>G
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