Canonical Allele Identifier: CA3710389
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1065600
gnomAD v2: 6-31237835-A-T
gnomAD v3: 6-31270058-A-T
gnomAD v4: 6-31270058-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270058A>T , CM000668.2:g.31270058A>T GRCh38
NC_000006.11:g.31237835A>T , CM000668.1:g.31237835A>T GRCh37
NC_000006.10:g.31345814A>T NCBI36
NG_029422.2:g.7074T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.923T>A MANE Select ENSP00000365402.5:p.Ile308Asn
ENST00000376228.9:c.923T>A ENSP00000365402.5:p.Ile308Asn
ENST00000376237.8:c.*510T>A ENSP00000365412.4:n.*510T>A
ENST00000383329.7:c.923T>A ENSP00000372819.3:p.Ile308Asn
ENST00000470363.5:n.241T>A
ENST00000487245.5:n.1282T>A
NM_002117.5:c.923T>A NP_002108.4:p.Ile308Asn
NM_002117.6:c.923T>A MANE Select NP_002108.4:p.Ile308Asn