Canonical Allele Identifier: CA137021925
Gene: HLA-DOA HGNC NCBI

Linked Data

dbSNP Id: rs367892819
gnomAD v2: 6-32972559-A-C
gnomAD v3: 6-33004782-A-C
gnomAD v4: 6-33004782-A-C
MyVariant Identifiers: chr6:g.32972559A>C (hg19) chr6:g.33004782A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33004782A>C , CM000668.2:g.33004782A>C GRCh38
NC_000006.11:g.32972559A>C , CM000668.1:g.32972559A>C GRCh37
NC_000006.10:g.33080537A>C NCBI36
NG_012007.1:g.9831T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000229829.7:c.*2056T>G MANE Select ENSP00000229829.3:n.*2056T>G
ENST00000229829.6:c.*2056T>G ENSP00000229829.3:n.*2056T>G
NM_002119.3:c.*2056T>G NP_002110.1:n.*2056T>G
NM_002119.4:c.*2056T>G MANE Select NP_002110.1:n.*2056T>G
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