Canonical Allele Identifier: CA12426132
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs9260106
gnomAD v2: 6-29909714-T-C
gnomAD v3: 6-29941937-T-C
gnomAD v4: 6-29941937-T-C
MyVariant Identifiers: chr6:g.29909714T>C (hg19) chr6:g.29941937T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29941937T>C , CM000668.2:g.29941937T>C GRCh38
NC_000006.11:g.29909714T>C , CM000668.1:g.29909714T>C GRCh37
NC_000006.10:g.30017693T>C NCBI36
NG_029217.2:g.4475T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000396634.5:c.-281-29T>C ENSP00000379873.1:n.-281-29T>C
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