Canonical Allele Identifier: CA935543131
Gene: OTOG HGNC NCBI

Linked Data

dbSNP Id: rs1851977212

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553026G>T , CM000673.2:g.17553026G>T GRCh38
NC_000011.9:g.17574573G>T , CM000673.1:g.17574573G>T GRCh37
NC_000011.8:g.17531149G>T NCBI36
NG_033191.1:g.10654G>T
NG_033191.2:g.10654G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.329-93G>T ENSP00000382323.2:n.329-93G>T
ENST00000399397.6:c.293-93G>T MANE Select ENSP00000382329.2:n.293-93G>T
ENST00000399391.6:c.329-93G>T ENSP00000382323.2:n.329-93G>T
ENST00000399397.5:c.293-93G>T ENSP00000382329.2:n.293-93G>T
ENST00000428619.1:c.110-93G>T ENSP00000399057.2:n.110-93G>T
ENST00000498332.5:n.199-93G>T
NM_001277269.1:c.329-93G>T NP_001264198.1:n.329-93G>T
NM_001292063.1:c.293-93G>T NP_001278992.1:n.293-93G>T
NM_001277269.2:c.329-93G>T NP_001264198.1:n.329-93G>T
NM_001292063.2:c.293-93G>T MANE Select NP_001278992.1:n.293-93G>T