Canonical Allele Identifier: CA12188681
Gene: HLA-DOB HGNC NCBI

Linked Data

dbSNP Id: rs17213693
gnomAD v2: 6-32781121-G-C
gnomAD v3: 6-32813344-G-C
gnomAD v4: 6-32813344-G-C
MyVariant Identifiers: chr6:g.32781121G>C (hg19) chr6:g.32813344G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32813344G>C , CM000668.2:g.32813344G>C GRCh38
NC_000006.11:g.32781121G>C , CM000668.1:g.32781121G>C GRCh37
NC_000006.10:g.32889099G>C NCBI36
NG_009793.3:g.30427C>G
NG_012008.1:g.8705C>G
NG_009793.4:g.30427C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000438763.7:c.787-93C>G MANE Select ENSP00000390020.2:n.787-93C>G
ENST00000648009.1:c.787-93C>G ENSP00000496848.1:n.787-93C>G
ENST00000438763.6:c.787-93C>G ENSP00000390020.2:n.787-93C>G
ENST00000475235.1:n.1310-93C>G
ENST00000488325.5:c.*558-93C>G ENSP00000436618.1:n.*558-93C>G
NM_002120.3:c.787-93C>G NP_002111.1:n.787-93C>G
NM_002120.4:c.787-93C>G MANE Select NP_002111.1:n.787-93C>G
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