Canonical Allele Identifier: CA2677950523
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31270128-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270128T>A , CM000668.2:g.31270128T>A GRCh38
NC_000006.11:g.31237905T>A , CM000668.1:g.31237905T>A GRCh37
NC_000006.10:g.31345884T>A NCBI36
NG_029422.2:g.7004A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.896-43A>T MANE Select ENSP00000365402.5:n.896-43A>T
ENST00000376228.9:c.896-43A>T ENSP00000365402.5:n.896-43A>T
ENST00000376237.8:c.*483-43A>T ENSP00000365412.4:n.*483-43A>T
ENST00000383329.7:c.896-43A>T ENSP00000372819.3:n.896-43A>T
ENST00000470363.5:n.214-43A>T
ENST00000487245.5:n.1255-43A>T
NM_002117.5:c.896-43A>T NP_002108.4:n.896-43A>T
NM_002117.6:c.896-43A>T MANE Select NP_002108.4:n.896-43A>T