Canonical Allele Identifier: CA823770157

Gene: HLA-A

Linked Data

• dbSNP Id: rs1449520999
• gnomAD v3: 6-29946089-A-C
• gnomAD v4: 6-29946089-A-C
• MyVariant Identifiers: chr6:g.29913866A>C (hg19) ; chr6:g.29946089A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29946089A>C , CM000668.2:g.29946089A>C	GRCh38
NC_000006.11:g.29913866A>C , CM000668.1:g.29913866A>C	GRCh37
NC_000006.10:g.30021845A>C	NCBI36
NG_029217.2:g.8625A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706901.1:c.*634A>C	ENSP00000516612.1:n.*634A>C
ENST00000706902.1:c.1093+808A>C	ENSP00000516613.1:n.1093+808A>C
ENST00000706903.1:c.*124+510A>C	ENSP00000516614.1:n.*124+510A>C
ENST00000706904.1:c.1093+808A>C	ENSP00000516615.1:n.1093+808A>C
ENST00000706905.1:c.*634A>C	ENSP00000516616.1:n.*634A>C