Canonical Allele Identifier: CA136866459

Gene: HLA-C

Linked Data

• dbSNP Id: rs281860535
• gnomAD v3: 6-31271117-A-G
• gnomAD v4: 6-31271117-A-G
• MyVariant Identifiers: chr6:g.31238894A>G (hg19) ; chr6:g.31271117A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271117A>G , CM000668.2:g.31271117A>G	GRCh38
NC_000006.11:g.31238894A>G , CM000668.1:g.31238894A>G	GRCh37
NC_000006.10:g.31346873A>G	NCBI36
NG_029422.2:g.6015T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.575T>C MANE Select	ENSP00000365402.5:p.Leu192Pro
ENST00000376228.9:c.575T>C	ENSP00000365402.5:p.Leu192Pro
ENST00000376237.8:c.*162T>C	ENSP00000365412.4:n.*162T>C
ENST00000383329.7:c.575T>C	ENSP00000372819.3:p.Leu192Pro
ENST00000415537.1:c.573T>C
ENST00000484378.1:n.844T>C
ENST00000487245.5:n.934T>C
ENST00000495835.1:n.764T>C
NM_002117.5:c.575T>C	NP_002108.4:p.Leu192Pro
NM_002117.6:c.575T>C MANE Select	NP_002108.4:p.Leu192Pro