Canonical Allele Identifier: CA3710342
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs775663281
gnomAD v2: 6-31237745-G-A
gnomAD v4: 6-31269968-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269968G>A , CM000668.2:g.31269968G>A GRCh38
NC_000006.11:g.31237745G>A , CM000668.1:g.31237745G>A GRCh37
NC_000006.10:g.31345724G>A NCBI36
NG_029422.2:g.7164C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1013C>T MANE Select ENSP00000365402.5:p.Ser338Leu
ENST00000376228.9:c.1013C>T ENSP00000365402.5:p.Ser338Leu
ENST00000376237.8:c.*600C>T ENSP00000365412.4:n.*600C>T
ENST00000383329.7:c.1013C>T ENSP00000372819.3:p.Ser338Leu
ENST00000470363.5:n.331C>T
ENST00000487245.5:n.1372C>T
NM_002117.5:c.1013C>T NP_002108.4:p.Ser338Leu
NM_002117.6:c.1013C>T MANE Select NP_002108.4:p.Ser338Leu