Canonical Allele Identifier: CA3710208

Gene: HLA-C

Linked Data

• dbSNP Id: rs3176007
• ExAC: 6:31236845 A / G
• gnomAD v2: 6-31236845-A-G
• gnomAD v3: 6-31269068-A-G
• gnomAD v4: 6-31269068-A-G
• MyVariant Identifiers: chr6:g.31236845A>G (hg19) ; chr6:g.31269068A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269068A>G , CM000668.2:g.31269068A>G	GRCh38
NC_000006.11:g.31236845A>G , CM000668.1:g.31236845A>G	GRCh37
NC_000006.10:g.31344824A>G	NCBI36
NG_029422.2:g.8064T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.*101T>C MANE Select	ENSP00000365402.5:n.*101T>C
ENST00000376228.9:c.*101T>C	ENSP00000365402.5:n.*101T>C
ENST00000376237.8:c.*789T>C	ENSP00000365412.4:n.*789T>C
ENST00000383329.7:c.*101T>C	ENSP00000372819.3:n.*101T>C
ENST00000466892.5:n.435T>C
ENST00000470363.5:n.960T>C
ENST00000487245.5:n.1561T>C
NM_002117.5:c.*101T>C	NP_002108.4:n.*101T>C
NM_002117.6:c.*101T>C MANE Select	NP_002108.4:n.*101T>C