Canonical Allele Identifier: CA824011831
Gene: HLA-DOA HGNC NCBI

Linked Data

dbSNP Id: rs1468244064
gnomAD v4: 6-33004640-G-T
MyVariant Identifiers: chr6:g.32972417G>T (hg19) chr6:g.33004640G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33004640G>T , CM000668.2:g.33004640G>T GRCh38
NC_000006.11:g.32972417G>T , CM000668.1:g.32972417G>T GRCh37
NC_000006.10:g.33080395G>T NCBI36
NG_012007.1:g.9973C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000229829.7:c.*2198C>A MANE Select ENSP00000229829.3:n.*2198C>A
ENST00000229829.6:c.*2198C>A ENSP00000229829.3:n.*2198C>A
NM_002119.3:c.*2198C>A NP_002110.1:n.*2198C>A
NM_002119.4:c.*2198C>A MANE Select NP_002110.1:n.*2198C>A
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