Canonical Allele Identifier: CA449790473

Gene: HLA-C

Linked Data

• dbSNP Id: rs281860408
• gnomAD v3: 6-31271651-A-G
• gnomAD v4: 6-31271651-A-G
• MyVariant Identifiers: chr6:g.31239428A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271651A>G , CM000668.2:g.31271651A>G	GRCh38
NC_000006.11:g.31239428A>G , CM000668.1:g.31239428A>G	GRCh37
NC_000006.10:g.31347407A>G	NCBI36
NG_029422.2:g.5481T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.291T>C MANE Select	ENSP00000365402.5:p.Ala97=
ENST00000376228.9:c.291T>C	ENSP00000365402.5:p.Ala97=
ENST00000376237.8:c.291T>C	ENSP00000365412.4:p.Ala97=
ENST00000383329.7:c.291T>C	ENSP00000372819.3:p.Ala97=
ENST00000415537.1:c.289T>C
ENST00000484378.1:n.310T>C
ENST00000487245.5:n.400T>C
ENST00000495835.1:n.480T>C
NM_002117.5:c.291T>C	NP_002108.4:p.Ala97=
NM_002117.6:c.291T>C MANE Select	NP_002108.4:p.Ala97=