Canonical Allele Identifier: CA449372397

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29942466-T-C
• MyVariant Identifiers: chr6:g.29910243T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942466T>C , CM000668.2:g.29942466T>C	GRCh38
NC_000006.11:g.29910243T>C , CM000668.1:g.29910243T>C	GRCh37
NC_000006.10:g.30018222T>C	NCBI36
NG_029217.2:g.5001T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706892.1:n.189T>C
ENST00000706893.1:c.-88T>C	ENSP00000516609.1:n.-88T>C
ENST00000706894.1:c.-88T>C	ENSP00000516610.1:n.-88T>C
ENST00000706895.1:n.189T>C
ENST00000706896.1:n.189T>C
ENST00000706897.1:n.189T>C
ENST00000706898.1:c.-88T>C	ENSP00000516611.1:n.-88T>C
ENST00000706899.1:n.189T>C
ENST00000706901.1:c.-88T>C	ENSP00000516612.1:n.-88T>C
ENST00000706902.1:c.-88T>C	ENSP00000516613.1:n.-88T>C
ENST00000706903.1:c.-88T>C	ENSP00000516614.1:n.-88T>C
ENST00000706904.1:c.-88T>C	ENSP00000516615.1:n.-88T>C
ENST00000706905.1:c.-88T>C	ENSP00000516616.1:n.-88T>C
ENST00000376806.9:c.-88T>C	ENSP00000366002.5:n.-88T>C
ENST00000396634.5:c.-88T>C	ENSP00000379873.1:n.-88T>C
ENST00000429656.1:n.602A>G