Canonical Allele Identifier: CA1619826699
Gene: HLA-DOA HGNC NCBI

Linked Data

dbSNP Id: rs1582978675
gnomAD v4: 6-33004719-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33004719T>C , CM000668.2:g.33004719T>C GRCh38
NC_000006.11:g.32972496T>C , CM000668.1:g.32972496T>C GRCh37
NC_000006.10:g.33080474T>C NCBI36
NG_012007.1:g.9894A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000229829.7:c.*2119A>G MANE Select ENSP00000229829.3:n.*2119A>G
ENST00000229829.6:c.*2119A>G ENSP00000229829.3:n.*2119A>G
NM_002119.3:c.*2119A>G NP_002110.1:n.*2119A>G
NM_002119.4:c.*2119A>G MANE Select NP_002110.1:n.*2119A>G
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