Canonical Allele Identifier: CA823770182
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs1418440971
gnomAD v3: 6-29946118-A-C
gnomAD v4: 6-29946118-A-C
MyVariant Identifiers: chr6:g.29913895A>C (hg19) chr6:g.29946118A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29946118A>C , CM000668.2:g.29946118A>C GRCh38
NC_000006.11:g.29913895A>C , CM000668.1:g.29913895A>C GRCh37
NC_000006.10:g.30021874A>C NCBI36
NG_029217.2:g.8654A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706901.1:c.*663A>C ENSP00000516612.1:n.*663A>C
ENST00000706902.1:c.1093+837A>C ENSP00000516613.1:n.1093+837A>C
ENST00000706903.1:c.*124+539A>C ENSP00000516614.1:n.*124+539A>C
ENST00000706904.1:c.1093+837A>C ENSP00000516615.1:n.1093+837A>C
ENST00000706905.1:c.*663A>C ENSP00000516616.1:n.*663A>C
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