Canonical Allele Identifier: CA136866942

Gene: HLA-C

Linked Data

• dbSNP Id: rs281860503
• gnomAD v4: 6-31271187-G-A
• MyVariant Identifiers: chr6:g.31238964G>A (hg19) ; chr6:g.31271187G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271187G>A , CM000668.2:g.31271187G>A	GRCh38
NC_000006.11:g.31238964G>A , CM000668.1:g.31238964G>A	GRCh37
NC_000006.10:g.31346943G>A	NCBI36
NG_029422.2:g.5945C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.505C>T MANE Select	ENSP00000365402.5:p.Arg169Cys
ENST00000376228.9:c.505C>T	ENSP00000365402.5:p.Arg169Cys
ENST00000376237.8:c.*92C>T	ENSP00000365412.4:n.*92C>T
ENST00000383329.7:c.505C>T	ENSP00000372819.3:p.Arg169Cys
ENST00000415537.1:c.503C>T
ENST00000484378.1:n.774C>T
ENST00000487245.5:n.864C>T
ENST00000495835.1:n.694C>T
NM_002117.5:c.505C>T	NP_002108.4:p.Arg169Cys
NM_002117.6:c.505C>T MANE Select	NP_002108.4:p.Arg169Cys