Canonical Allele Identifier: CA137021901
Gene: HLA-DOA HGNC NCBI

Linked Data

dbSNP Id: rs543748753
gnomAD v2: 6-32972516-G-A
gnomAD v3: 6-33004739-G-A
gnomAD v4: 6-33004739-G-A
MyVariant Identifiers: chr6:g.32972516G>A (hg19) chr6:g.33004739G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33004739G>A , CM000668.2:g.33004739G>A GRCh38
NC_000006.11:g.32972516G>A , CM000668.1:g.32972516G>A GRCh37
NC_000006.10:g.33080494G>A NCBI36
NG_012007.1:g.9874C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000229829.7:c.*2099C>T MANE Select ENSP00000229829.3:n.*2099C>T
ENST00000229829.6:c.*2099C>T ENSP00000229829.3:n.*2099C>T
NM_002119.3:c.*2099C>T NP_002110.1:n.*2099C>T
NM_002119.4:c.*2099C>T MANE Select NP_002110.1:n.*2099C>T
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