Canonical Allele Identifier: CA2677950099
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269795-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269795T>A , CM000668.2:g.31269795T>A GRCh38
NC_000006.11:g.31237572T>A , CM000668.1:g.31237572T>A GRCh37
NC_000006.10:g.31345551T>A NCBI36
NG_029422.2:g.7337A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1015+171A>T MANE Select ENSP00000365402.5:n.1015+171A>T
ENST00000376228.9:c.1015+171A>T ENSP00000365402.5:n.1015+171A>T
ENST00000376237.8:c.*602+171A>T ENSP00000365412.4:n.*602+171A>T
ENST00000383329.7:c.1015+171A>T ENSP00000372819.3:n.1015+171A>T
ENST00000470363.5:n.504A>T
ENST00000487245.5:n.1374+171A>T
NM_002117.5:c.1015+171A>T NP_002108.4:n.1015+171A>T
NM_002117.6:c.1015+171A>T MANE Select NP_002108.4:n.1015+171A>T