Canonical Allele Identifier: CA136986650

Gene: HLA-DOB

Linked Data

• dbSNP Id: rs1028362020
• gnomAD v3: 6-32813363-C-T
• gnomAD v4: 6-32813363-C-T
• MyVariant Identifiers: chr6:g.32781140C>T (hg19) ; chr6:g.32813363C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32813363C>T , CM000668.2:g.32813363C>T	GRCh38
NC_000006.11:g.32781140C>T , CM000668.1:g.32781140C>T	GRCh37
NC_000006.10:g.32889118C>T	NCBI36
NG_009793.3:g.30408G>A
NG_012008.1:g.8686G>A
NG_009793.4:g.30408G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000438763.7:c.786+77G>A MANE Select	ENSP00000390020.2:n.786+77G>A
ENST00000648009.1:c.786+77G>A	ENSP00000496848.1:n.786+77G>A
ENST00000438763.6:c.786+77G>A	ENSP00000390020.2:n.786+77G>A
ENST00000475235.1:n.1309+77G>A
ENST00000488325.5:c.*557+77G>A	ENSP00000436618.1:n.*557+77G>A
NM_002120.3:c.786+77G>A	NP_002111.1:n.786+77G>A
NM_002120.4:c.786+77G>A MANE Select	NP_002111.1:n.786+77G>A