Canonical Allele Identifier: CA915283667
Gene: HLA-DOA HGNC NCBI

Linked Data

dbSNP Id: rs1562006571
gnomAD v2: 6-32972523-T-C
gnomAD v3: 6-33004746-T-C
gnomAD v4: 6-33004746-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33004746T>C , CM000668.2:g.33004746T>C GRCh38
NC_000006.11:g.32972523T>C , CM000668.1:g.32972523T>C GRCh37
NC_000006.10:g.33080501T>C NCBI36
NG_012007.1:g.9867A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000229829.7:c.*2092A>G MANE Select ENSP00000229829.3:n.*2092A>G
ENST00000229829.6:c.*2092A>G ENSP00000229829.3:n.*2092A>G
NM_002119.3:c.*2092A>G NP_002110.1:n.*2092A>G
NM_002119.4:c.*2092A>G MANE Select NP_002110.1:n.*2092A>G