Canonical Allele Identifier: CA379786327
Gene: OTOG HGNC NCBI

Linked Data

gnomAD v4: 11-17642133-G-A
MyVariant Identifiers: chr11:g.17663680G>A (hg19) chr11:g.17642133G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17642133G>A , CM000673.2:g.17642133G>A GRCh38
NC_000011.9:g.17663680G>A , CM000673.1:g.17663680G>A GRCh37
NC_000011.8:g.17620256G>A NCBI36
NG_033191.1:g.99761G>A
NG_033191.2:g.99761G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.8338G>A ENSP00000382323.2:p.Ala2780Thr
ENST00000399397.6:c.8302G>A MANE Select ENSP00000382329.2:p.Ala2768Thr
ENST00000399391.6:c.8338G>A ENSP00000382323.2:p.Ala2780Thr
ENST00000399397.5:c.8302G>A ENSP00000382329.2:p.Ala2768Thr
NM_001277269.1:c.8338G>A NP_001264198.1:p.Ala2780Thr
NM_001292063.1:c.8302G>A NP_001278992.1:p.Ala2768Thr
NM_001277269.2:c.8338G>A NP_001264198.1:p.Ala2780Thr
NM_001292063.2:c.8302G>A MANE Select NP_001278992.1:p.Ala2768Thr
Search 100 bp 5'
Search 100 bp 3'