Canonical Allele Identifier: CA823770099
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs1240161474
gnomAD v3: 6-29945988-G-T
gnomAD v4: 6-29945988-G-T
MyVariant Identifiers: chr6:g.29913765G>T (hg19) chr6:g.29945988G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945988G>T , CM000668.2:g.29945988G>T GRCh38
NC_000006.11:g.29913765G>T , CM000668.1:g.29913765G>T GRCh37
NC_000006.10:g.30021744G>T NCBI36
NG_029217.2:g.8524G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706901.1:c.*533G>T ENSP00000516612.1:n.*533G>T
ENST00000706902.1:c.1093+707G>T ENSP00000516613.1:n.1093+707G>T
ENST00000706903.1:c.*124+409G>T ENSP00000516614.1:n.*124+409G>T
ENST00000706904.1:c.1093+707G>T ENSP00000516615.1:n.1093+707G>T
ENST00000706905.1:c.*533G>T ENSP00000516616.1:n.*533G>T
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