Canonical Allele Identifier: CA3745520
Gene: HLA-DOB HGNC NCBI

Linked Data

dbSNP Id: rs373980828
ExAC: 6:32782037 C / G
gnomAD v2: 6-32782037-C-G
gnomAD v3: 6-32814260-C-G
gnomAD v4: 6-32814260-C-G
MyVariant Identifiers: chr6:g.32782037C>G (hg19) chr6:g.32814260C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32814260C>G , CM000668.2:g.32814260C>G GRCh38
NC_000006.11:g.32782037C>G , CM000668.1:g.32782037C>G GRCh37
NC_000006.10:g.32890015C>G NCBI36
NG_009793.3:g.29511G>C
NG_012008.1:g.7789G>C
NG_009793.4:g.29511G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000438763.7:c.643+60G>C MANE Select ENSP00000390020.2:n.643+60G>C
ENST00000648009.1:c.643+60G>C ENSP00000496848.1:n.643+60G>C
ENST00000438763.6:c.643+60G>C ENSP00000390020.2:n.643+60G>C
ENST00000452392.2:c.2464+60G>C ENSP00000391806.2:n.2464+60G>C
ENST00000475235.1:n.740G>C
ENST00000488325.5:c.*414+60G>C ENSP00000436618.1:n.*414+60G>C
NM_002120.3:c.643+60G>C NP_002111.1:n.643+60G>C
NM_002120.4:c.643+60G>C MANE Select NP_002111.1:n.643+60G>C
Search 100 bp 5'
Search 100 bp 3'