Canonical Allele Identifier: CA1619080169
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs9264647
gnomAD v4: 6-31270836-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270836A>C , CM000668.2:g.31270836A>C GRCh38
NC_000006.11:g.31238613A>C , CM000668.1:g.31238613A>C GRCh37
NC_000006.10:g.31346592A>C NCBI36
NG_029422.2:g.6296T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.619+237T>G MANE Select ENSP00000365402.5:n.619+237T>G
ENST00000376228.9:c.619+237T>G ENSP00000365402.5:n.619+237T>G
ENST00000376237.8:c.*206+237T>G ENSP00000365412.4:n.*206+237T>G
ENST00000383329.7:c.619+237T>G ENSP00000372819.3:n.619+237T>G
ENST00000415537.1:c.617+237T>G
ENST00000487245.5:n.978+237T>G
ENST00000495835.1:n.808+237T>G
NM_002117.5:c.619+237T>G NP_002108.4:n.619+237T>G
NM_002117.6:c.619+237T>G MANE Select NP_002108.4:n.619+237T>G
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