Canonical Allele Identifier: CA449790011

Gene: HLA-C

Linked Data

• MyVariant Identifiers: chr6:g.31237822A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270045A>T , CM000668.2:g.31270045A>T	GRCh38
NC_000006.11:g.31237822A>T , CM000668.1:g.31237822A>T	GRCh37
NC_000006.10:g.31345801A>T	NCBI36
NG_029422.2:g.7087T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.936T>A MANE Select	ENSP00000365402.5:p.Val312=
ENST00000376228.9:c.936T>A	ENSP00000365402.5:p.Val312=
ENST00000376237.8:c.*523T>A	ENSP00000365412.4:n.*523T>A
ENST00000383329.7:c.936T>A	ENSP00000372819.3:p.Val312=
ENST00000470363.5:n.254T>A
ENST00000487245.5:n.1295T>A
NM_002117.5:c.936T>A	NP_002108.4:p.Val312=
NM_002117.6:c.936T>A MANE Select	NP_002108.4:p.Val312=