Canonical Allele Identifier: CA136987391
Gene: HLA-DOB HGNC NCBI

Linked Data

dbSNP Id: rs1013075650
gnomAD v4: 6-32814199-C-T
MyVariant Identifiers: chr6:g.32781976C>T (hg19) chr6:g.32814199C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32814199C>T , CM000668.2:g.32814199C>T GRCh38
NC_000006.11:g.32781976C>T , CM000668.1:g.32781976C>T GRCh37
NC_000006.10:g.32889954C>T NCBI36
NG_009793.3:g.29572G>A
NG_012008.1:g.7850G>A
NG_009793.4:g.29572G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000438763.7:c.643+121G>A MANE Select ENSP00000390020.2:n.643+121G>A
ENST00000648009.1:c.643+121G>A ENSP00000496848.1:n.643+121G>A
ENST00000438763.6:c.643+121G>A ENSP00000390020.2:n.643+121G>A
ENST00000452392.2:c.2464+121G>A ENSP00000391806.2:n.2464+121G>A
ENST00000475235.1:n.801G>A
ENST00000488325.5:c.*414+121G>A ENSP00000436618.1:n.*414+121G>A
NM_002120.3:c.643+121G>A NP_002111.1:n.643+121G>A
NM_002120.4:c.643+121G>A MANE Select NP_002111.1:n.643+121G>A
Search 100 bp 5'
Search 100 bp 3'