Canonical Allele Identifier: CA1087616801
Gene: HLA-DOB HGNC NCBI

Linked Data

dbSNP Id: rs1767917959
gnomAD v3: 6-32814225-T-C
gnomAD v4: 6-32814225-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32814225T>C , CM000668.2:g.32814225T>C GRCh38
NC_000006.11:g.32782002T>C , CM000668.1:g.32782002T>C GRCh37
NC_000006.10:g.32889980T>C NCBI36
NG_009793.3:g.29546A>G
NG_012008.1:g.7824A>G
NG_009793.4:g.29546A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000438763.7:c.643+95A>G MANE Select ENSP00000390020.2:n.643+95A>G
ENST00000648009.1:c.643+95A>G ENSP00000496848.1:n.643+95A>G
ENST00000438763.6:c.643+95A>G ENSP00000390020.2:n.643+95A>G
ENST00000452392.2:c.2464+95A>G ENSP00000391806.2:n.2464+95A>G
ENST00000475235.1:n.775A>G
ENST00000488325.5:c.*414+95A>G ENSP00000436618.1:n.*414+95A>G
NM_002120.3:c.643+95A>G NP_002111.1:n.643+95A>G
NM_002120.4:c.643+95A>G MANE Select NP_002111.1:n.643+95A>G