Canonical Allele Identifier: CA449373002

Gene: HLA-A

Linked Data

• dbSNP Id: rs199780123
• gnomAD v3: 6-29942512-G-A
• gnomAD v4: 6-29942512-G-A
• MyVariant Identifiers: chr6:g.29910289G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942512G>A , CM000668.2:g.29942512G>A	GRCh38
NC_000006.11:g.29910289G>A , CM000668.1:g.29910289G>A	GRCh37
NC_000006.10:g.30018268G>A	NCBI36
NG_029217.2:g.5047G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706892.1:n.235G>A
ENST00000706893.1:c.-42G>A	ENSP00000516609.1:n.-42G>A
ENST00000706894.1:c.-42G>A	ENSP00000516610.1:n.-42G>A
ENST00000706895.1:n.235G>A
ENST00000706896.1:n.235G>A
ENST00000706897.1:n.235G>A
ENST00000706898.1:c.-42G>A	ENSP00000516611.1:n.-42G>A
ENST00000706899.1:n.235G>A
ENST00000706901.1:c.-42G>A	ENSP00000516612.1:n.-42G>A
ENST00000706902.1:c.-42G>A	ENSP00000516613.1:n.-42G>A
ENST00000706903.1:c.-42G>A	ENSP00000516614.1:n.-42G>A
ENST00000706904.1:c.-42G>A	ENSP00000516615.1:n.-42G>A
ENST00000706905.1:c.-42G>A	ENSP00000516616.1:n.-42G>A
ENST00000376806.9:c.-42G>A	ENSP00000366002.5:n.-42G>A
ENST00000376809.9:c.-42G>A	ENSP00000366005.5:n.-42G>A
ENST00000396634.5:c.-42G>A	ENSP00000379873.1:n.-42G>A
ENST00000429656.1:n.556C>T
NM_002116.7:c.-42G>A	NP_002107.3:n.-42G>A