Canonical Allele Identifier: CA363324496

Gene: HLA-C

Linked Data

• dbSNP Id: rs77935220
• gnomAD v3: 6-31271109-A-C
• gnomAD v4: 6-31271109-A-C
• MyVariant Identifiers: chr6:g.31238886A>C (hg19) ; chr6:g.31271109A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271109A>C , CM000668.2:g.31271109A>C	GRCh38
NC_000006.11:g.31238886A>C , CM000668.1:g.31238886A>C	GRCh37
NC_000006.10:g.31346865A>C	NCBI36
NG_029422.2:g.6023T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.583T>G MANE Select	ENSP00000365402.5:p.Tyr195Asp
ENST00000376228.9:c.583T>G	ENSP00000365402.5:p.Tyr195Asp
ENST00000376237.8:c.*170T>G	ENSP00000365412.4:n.*170T>G
ENST00000383329.7:c.583T>G	ENSP00000372819.3:p.Tyr195Asp
ENST00000415537.1:c.581T>G
ENST00000484378.1:n.852T>G
ENST00000487245.5:n.942T>G
ENST00000495835.1:n.772T>G
NM_002117.5:c.583T>G	NP_002108.4:p.Tyr195Asp
NM_002117.6:c.583T>G MANE Select	NP_002108.4:p.Tyr195Asp