Canonical Allele Identifier: CA3710262
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs751964800
gnomAD v2: 6-31237131-A-G
gnomAD v3: 6-31269354-A-G
gnomAD v4: 6-31269354-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269354A>G , CM000668.2:g.31269354A>G GRCh38
NC_000006.11:g.31237131A>G , CM000668.1:g.31237131A>G GRCh37
NC_000006.10:g.31345110A>G NCBI36
NG_029422.2:g.7778T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1080T>C MANE Select ENSP00000365402.5:p.Ser360=
ENST00000376228.9:c.1080T>C ENSP00000365402.5:p.Ser360=
ENST00000376237.8:c.*667T>C ENSP00000365412.4:n.*667T>C
ENST00000383329.7:c.1098T>C ENSP00000372819.3:p.Ser366=
ENST00000466892.5:n.313T>C
ENST00000470363.5:n.838T>C
ENST00000487245.5:n.1439T>C
NM_002117.5:c.1080T>C NP_002108.4:p.Ser360=
NM_002117.6:c.1080T>C MANE Select NP_002108.4:p.Ser360=