Canonical Allele Identifier: CA136017345
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs376055041
gnomAD v2: 6-29909725-T-G
gnomAD v3: 6-29941948-T-G
gnomAD v4: 6-29941948-T-G
MyVariant Identifiers: chr6:g.29909725T>G (hg19) chr6:g.29941948T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29941948T>G , CM000668.2:g.29941948T>G GRCh38
NC_000006.11:g.29909725T>G , CM000668.1:g.29909725T>G GRCh37
NC_000006.10:g.30017704T>G NCBI36
NG_029217.2:g.4486T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000396634.5:c.-281-18T>G ENSP00000379873.1:n.-281-18T>G
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