Canonical Allele Identifier: CA449370307

Gene: HLA-A

Linked Data

• dbSNP Id: rs2127581652
• gnomAD v4: 6-29942248-T-C
• MyVariant Identifiers: chr6:g.29910025T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942248T>C , CM000668.2:g.29942248T>C	GRCh38
NC_000006.11:g.29910025T>C , CM000668.1:g.29910025T>C	GRCh37
NC_000006.10:g.30018004T>C	NCBI36
NG_029217.2:g.4783T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706892.1:n.126+152T>C
ENST00000706893.1:c.-151+152T>C	ENSP00000516609.1:n.-151+152T>C
ENST00000706894.1:c.-151+152T>C	ENSP00000516610.1:n.-151+152T>C
ENST00000706895.1:n.126+152T>C
ENST00000706896.1:n.126+152T>C
ENST00000706897.1:n.126+152T>C
ENST00000706898.1:c.-151+152T>C	ENSP00000516611.1:n.-151+152T>C
ENST00000706899.1:n.126+152T>C
ENST00000706901.1:c.-151+152T>C	ENSP00000516612.1:n.-151+152T>C
ENST00000706902.1:c.-151+152T>C	ENSP00000516613.1:n.-151+152T>C
ENST00000706903.1:c.-151+152T>C	ENSP00000516614.1:n.-151+152T>C
ENST00000706904.1:c.-151+152T>C	ENSP00000516615.1:n.-151+152T>C
ENST00000376806.9:c.-306T>C	ENSP00000366002.5:n.-306T>C
ENST00000396634.5:c.-151+152T>C	ENSP00000379873.1:n.-151+152T>C
ENST00000429656.1:n.820A>G