Canonical Allele Identifier: CA363319294
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1181702895
gnomAD v2: 6-31237142-A-T
gnomAD v4: 6-31269365-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269365A>T , CM000668.2:g.31269365A>T GRCh38
NC_000006.11:g.31237142A>T , CM000668.1:g.31237142A>T GRCh37
NC_000006.10:g.31345121A>T NCBI36
NG_029422.2:g.7767T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1069T>A MANE Select ENSP00000365402.5:p.Ser357Thr
ENST00000376228.9:c.1069T>A ENSP00000365402.5:p.Ser357Thr
ENST00000376237.8:c.*656T>A ENSP00000365412.4:n.*656T>A
ENST00000383329.7:c.1087T>A ENSP00000372819.3:p.Ser363Thr
ENST00000466892.5:n.302T>A
ENST00000470363.5:n.827T>A
ENST00000487245.5:n.1428T>A
NM_002117.5:c.1069T>A NP_002108.4:p.Ser357Thr
NM_002117.6:c.1069T>A MANE Select NP_002108.4:p.Ser357Thr