Canonical Allele Identifier: CA449746490
Gene: HLA-DOB HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.32781017A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32813240A>T , CM000668.2:g.32813240A>T GRCh38
NC_000006.11:g.32781017A>T , CM000668.1:g.32781017A>T GRCh37
NC_000006.10:g.32888995A>T NCBI36
NG_009793.3:g.30531T>A
NG_012008.1:g.8809T>A
NG_009793.4:g.30531T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000438763.7:c.798T>A MANE Select ENSP00000390020.2:p.Ala266=
ENST00000648009.1:c.798T>A ENSP00000496848.1:p.Ala266=
ENST00000438763.6:c.798T>A ENSP00000390020.2:p.Ala266=
ENST00000475235.1:n.1321T>A
ENST00000488325.5:c.*569T>A ENSP00000436618.1:n.*569T>A
NM_002120.3:c.798T>A NP_002111.1:p.Ala266=
NM_002120.4:c.798T>A MANE Select NP_002111.1:p.Ala266=