Canonical Allele Identifier: CA3710735

Gene: HLA-C

Linked Data

• dbSNP Id: rs281860494
• ExAC: 6:31238989 C / G
• gnomAD v2: 6-31238989-C-G
• gnomAD v4: 6-31271212-C-G
• MyVariant Identifiers: chr6:g.31238989C>G (hg19) ; chr6:g.31271212C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271212C>G , CM000668.2:g.31271212C>G	GRCh38
NC_000006.11:g.31238989C>G , CM000668.1:g.31238989C>G	GRCh37
NC_000006.10:g.31346968C>G	NCBI36
NG_029422.2:g.5920G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.480G>C MANE Select	ENSP00000365402.5:p.Ala160=
ENST00000376228.9:c.480G>C	ENSP00000365402.5:p.Ala160=
ENST00000376237.8:c.*67G>C	ENSP00000365412.4:n.*67G>C
ENST00000383329.7:c.480G>C	ENSP00000372819.3:p.Ala160=
ENST00000415537.1:c.478G>C
ENST00000484378.1:n.749G>C
ENST00000487245.5:n.839G>C
ENST00000495835.1:n.669G>C
NM_002117.5:c.480G>C	NP_002108.4:p.Ala160=
NM_002117.6:c.480G>C MANE Select	NP_002108.4:p.Ala160=