Canonical Allele Identifier: CA136867631

Gene: HLA-C

Linked Data

• dbSNP Id: rs41562320
• gnomAD v4: 6-31271286-C-G
• MyVariant Identifiers: chr6:g.31239063C>G (hg19) ; chr6:g.31271286C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271286C>G , CM000668.2:g.31271286C>G	GRCh38
NC_000006.11:g.31239063C>G , CM000668.1:g.31239063C>G	GRCh37
NC_000006.10:g.31347042C>G	NCBI36
NG_029422.2:g.5846G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.406G>C MANE Select	ENSP00000365402.5:p.Gly136Arg
ENST00000376228.9:c.406G>C	ENSP00000365402.5:p.Gly136Arg
ENST00000376237.8:c.389G>C	ENSP00000365412.4:p.Arg130Pro
ENST00000383329.7:c.406G>C	ENSP00000372819.3:p.Gly136Arg
ENST00000415537.1:c.404G>C
ENST00000484378.1:n.675G>C
ENST00000487245.5:n.765G>C
ENST00000495835.1:n.595G>C
NM_002117.5:c.406G>C	NP_002108.4:p.Gly136Arg
NM_002117.6:c.406G>C MANE Select	NP_002108.4:p.Gly136Arg