Canonical Allele Identifier: CA136017473

Gene: HLA-A

Linked Data

• dbSNP Id: rs182864342
• gnomAD v2: 6-29909911-G-A
• gnomAD v3: 6-29942134-G-A
• gnomAD v4: 6-29942134-G-A
• MyVariant Identifiers: chr6:g.29909911G>A (hg19) ; chr6:g.29942134G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942134G>A , CM000668.2:g.29942134G>A	GRCh38
NC_000006.11:g.29909911G>A , CM000668.1:g.29909911G>A	GRCh37
NC_000006.10:g.30017890G>A	NCBI36
NG_029217.2:g.4669G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706892.1:n.126+38G>A
ENST00000706893.1:c.-151+38G>A	ENSP00000516609.1:n.-151+38G>A
ENST00000706894.1:c.-151+38G>A	ENSP00000516610.1:n.-151+38G>A
ENST00000706895.1:n.126+38G>A
ENST00000706896.1:n.126+38G>A
ENST00000706897.1:n.126+38G>A
ENST00000706898.1:c.-151+38G>A	ENSP00000516611.1:n.-151+38G>A
ENST00000706899.1:n.126+38G>A
ENST00000706901.1:c.-151+38G>A	ENSP00000516612.1:n.-151+38G>A
ENST00000706902.1:c.-151+38G>A	ENSP00000516613.1:n.-151+38G>A
ENST00000706903.1:c.-151+38G>A	ENSP00000516614.1:n.-151+38G>A
ENST00000706904.1:c.-151+38G>A	ENSP00000516615.1:n.-151+38G>A
ENST00000396634.5:c.-151+38G>A	ENSP00000379873.1:n.-151+38G>A
ENST00000429656.1:n.934C>T