Canonical Allele Identifier: CA136026153
Gene: HLA-A HGNC NCBI

Linked Data

dbSNP Id: rs796344137 rs2127259534
gnomAD v2: 6-29913945-A-G
gnomAD v3: 6-29946168-A-G
gnomAD v4: 6-29946168-A-G
MyVariant Identifiers: chr6:g.29913945A>G (hg19) chr6:g.29946168A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29946168A>G , CM000668.2:g.29946168A>G GRCh38
NC_000006.11:g.29913945A>G , CM000668.1:g.29913945A>G GRCh37
NC_000006.10:g.30021924A>G NCBI36
NG_029217.2:g.8704A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706901.1:c.*713A>G ENSP00000516612.1:n.*713A>G
ENST00000706902.1:c.1093+887A>G ENSP00000516613.1:n.1093+887A>G
ENST00000706903.1:c.*124+589A>G ENSP00000516614.1:n.*124+589A>G
ENST00000706904.1:c.1093+887A>G ENSP00000516615.1:n.1093+887A>G
ENST00000706905.1:c.*713A>G ENSP00000516616.1:n.*713A>G
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