Canonical Allele Identifier: CA2677949118
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31268915-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268915T>A , CM000668.2:g.31268915T>A GRCh38
NC_000006.11:g.31236692T>A , CM000668.1:g.31236692T>A GRCh37
NC_000006.10:g.31344671T>A NCBI36
NG_029422.2:g.8217A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*254A>T MANE Select ENSP00000365402.5:n.*254A>T
ENST00000376228.9:c.*254A>T ENSP00000365402.5:n.*254A>T
ENST00000376237.8:c.*942A>T ENSP00000365412.4:n.*942A>T
ENST00000383329.7:c.*254A>T ENSP00000372819.3:n.*254A>T
ENST00000466892.5:n.588A>T
ENST00000470363.5:n.1113A>T
ENST00000487245.5:n.1714A>T
NM_002117.5:c.*254A>T NP_002108.4:n.*254A>T
NM_002117.6:c.*254A>T MANE Select NP_002108.4:n.*254A>T