Canonical Allele Identifier: CA565893759
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs1281381935 rs2127259454
gnomAD v2: 6-29913871-A-C
gnomAD v3: 6-29946094-A-C
gnomAD v4: 6-29946094-A-C
MyVariant Identifiers: chr6:g.29913871A>C (hg19) chr6:g.29946094A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29946094A>C , CM000668.2:g.29946094A>C GRCh38
NC_000006.11:g.29913871A>C , CM000668.1:g.29913871A>C GRCh37
NC_000006.10:g.30021850A>C NCBI36
NG_029217.2:g.8630A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706901.1:c.*639A>C ENSP00000516612.1:n.*639A>C
ENST00000706902.1:c.1093+813A>C ENSP00000516613.1:n.1093+813A>C
ENST00000706903.1:c.*124+515A>C ENSP00000516614.1:n.*124+515A>C
ENST00000706904.1:c.1093+813A>C ENSP00000516615.1:n.1093+813A>C
ENST00000706905.1:c.*639A>C ENSP00000516616.1:n.*639A>C
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