Canonical Allele Identifier: CA3692816

Gene: HLA-A

Linked Data

• dbSNP Id: rs778788809
• ExAC: 6:29910293 G / A
• gnomAD v2: 6-29910293-G-A
• gnomAD v3: 6-29942516-G-A
• gnomAD v4: 6-29942516-G-A
• MyVariant Identifiers: chr6:g.29910293G>A (hg19) ; chr6:g.29942516G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942516G>A , CM000668.2:g.29942516G>A	GRCh38
NC_000006.11:g.29910293G>A , CM000668.1:g.29910293G>A	GRCh37
NC_000006.10:g.30018272G>A	NCBI36
NG_029217.2:g.5051G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706892.1:n.239G>A
ENST00000706893.1:c.-38G>A	ENSP00000516609.1:n.-38G>A
ENST00000706894.1:c.-38G>A	ENSP00000516610.1:n.-38G>A
ENST00000706895.1:n.239G>A
ENST00000706896.1:n.239G>A
ENST00000706897.1:n.239G>A
ENST00000706898.1:c.-38G>A	ENSP00000516611.1:n.-38G>A
ENST00000706899.1:n.239G>A
ENST00000706901.1:c.-38G>A	ENSP00000516612.1:n.-38G>A
ENST00000706902.1:c.-38G>A	ENSP00000516613.1:n.-38G>A
ENST00000706903.1:c.-38G>A	ENSP00000516614.1:n.-38G>A
ENST00000706904.1:c.-38G>A	ENSP00000516615.1:n.-38G>A
ENST00000706905.1:c.-38G>A	ENSP00000516616.1:n.-38G>A
ENST00000376806.9:c.-38G>A	ENSP00000366002.5:n.-38G>A
ENST00000376809.9:c.-38G>A	ENSP00000366005.5:n.-38G>A
ENST00000396634.5:c.-38G>A	ENSP00000379873.1:n.-38G>A
ENST00000429656.1:n.552C>T
NM_002116.7:c.-38G>A	NP_002107.3:n.-38G>A