Canonical Allele Identifier: CA12230070

Gene: HLA-A

Linked Data

• dbSNP Id: rs2735115
• gnomAD v2: 6-29910022-C-A
• gnomAD v3: 6-29942245-C-A
• gnomAD v4: 6-29942245-C-A
• MyVariant Identifiers: chr6:g.29910022C>A (hg19) ; chr6:g.29942245C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942245C>A , CM000668.2:g.29942245C>A	GRCh38
NC_000006.11:g.29910022C>A , CM000668.1:g.29910022C>A	GRCh37
NC_000006.10:g.30018001C>A	NCBI36
NG_029217.2:g.4780C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000706892.1:n.126+149C>A
ENST00000706893.1:c.-151+149C>A	ENSP00000516609.1:n.-151+149C>A
ENST00000706894.1:c.-151+149C>A	ENSP00000516610.1:n.-151+149C>A
ENST00000706895.1:n.126+149C>A
ENST00000706896.1:n.126+149C>A
ENST00000706897.1:n.126+149C>A
ENST00000706898.1:c.-151+149C>A	ENSP00000516611.1:n.-151+149C>A
ENST00000706899.1:n.126+149C>A
ENST00000706901.1:c.-151+149C>A	ENSP00000516612.1:n.-151+149C>A
ENST00000706902.1:c.-151+149C>A	ENSP00000516613.1:n.-151+149C>A
ENST00000706903.1:c.-151+149C>A	ENSP00000516614.1:n.-151+149C>A
ENST00000706904.1:c.-151+149C>A	ENSP00000516615.1:n.-151+149C>A
ENST00000376806.9:c.-309C>A	ENSP00000366002.5:n.-309C>A
ENST00000396634.5:c.-151+149C>A	ENSP00000379873.1:n.-151+149C>A
ENST00000429656.1:n.823G>T