Canonical Allele Identifier: CA3710420

Gene: HLA-C

Linked Data

• dbSNP Id: rs767135148
• ExAC: 6:31237951 C / G
• gnomAD v2: 6-31237951-C-G
• MyVariant Identifiers: chr6:g.31237951C>G (hg19) ; chr6:g.31270174C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31270174C>G , CM000668.2:g.31270174C>G	GRCh38
NC_000006.11:g.31237951C>G , CM000668.1:g.31237951C>G	GRCh37
NC_000006.10:g.31345930C>G	NCBI36
NG_029422.2:g.6958G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.895+36G>C MANE Select	ENSP00000365402.5:n.895+36G>C
ENST00000376228.9:c.895+36G>C	ENSP00000365402.5:n.895+36G>C
ENST00000376237.8:c.*482+36G>C	ENSP00000365412.4:n.*482+36G>C
ENST00000383329.7:c.895+36G>C	ENSP00000372819.3:n.895+36G>C
ENST00000470363.5:n.213+36G>C
ENST00000487245.5:n.1254+36G>C
NM_002117.5:c.895+36G>C	NP_002108.4:n.895+36G>C
NM_002117.6:c.895+36G>C MANE Select	NP_002108.4:n.895+36G>C