Canonical Allele Identifier: CA449370374

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29942255-A-G
• MyVariant Identifiers: chr6:g.29910032A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942255A>G , CM000668.2:g.29942255A>G	GRCh38
NC_000006.11:g.29910032A>G , CM000668.1:g.29910032A>G	GRCh37
NC_000006.10:g.30018011A>G	NCBI36
NG_029217.2:g.4790A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000706892.1:n.127-149A>G
ENST00000706893.1:c.-150-149A>G	ENSP00000516609.1:n.-150-149A>G
ENST00000706894.1:c.-150-149A>G	ENSP00000516610.1:n.-150-149A>G
ENST00000706895.1:n.127-149A>G
ENST00000706896.1:n.127-149A>G
ENST00000706897.1:n.127-149A>G
ENST00000706898.1:c.-150-149A>G	ENSP00000516611.1:n.-150-149A>G
ENST00000706899.1:n.127-149A>G
ENST00000706901.1:c.-150-149A>G	ENSP00000516612.1:n.-150-149A>G
ENST00000706902.1:c.-150-149A>G	ENSP00000516613.1:n.-150-149A>G
ENST00000706903.1:c.-150-149A>G	ENSP00000516614.1:n.-150-149A>G
ENST00000706904.1:c.-150-149A>G	ENSP00000516615.1:n.-150-149A>G
ENST00000376806.9:c.-299A>G	ENSP00000366002.5:n.-299A>G
ENST00000396634.5:c.-150-149A>G	ENSP00000379873.1:n.-150-149A>G
ENST00000429656.1:n.813T>C