Canonical Allele Identifier: CA2677950095
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269792-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269792T>C , CM000668.2:g.31269792T>C GRCh38
NC_000006.11:g.31237569T>C , CM000668.1:g.31237569T>C GRCh37
NC_000006.10:g.31345548T>C NCBI36
NG_029422.2:g.7340A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1015+174A>G MANE Select ENSP00000365402.5:n.1015+174A>G
ENST00000376228.9:c.1015+174A>G ENSP00000365402.5:n.1015+174A>G
ENST00000376237.8:c.*602+174A>G ENSP00000365412.4:n.*602+174A>G
ENST00000383329.7:c.1015+174A>G ENSP00000372819.3:n.1015+174A>G
ENST00000470363.5:n.507A>G
ENST00000487245.5:n.1374+174A>G
NM_002117.5:c.1015+174A>G NP_002108.4:n.1015+174A>G
NM_002117.6:c.1015+174A>G MANE Select NP_002108.4:n.1015+174A>G