Canonical Allele Identifier: CA935548973

Gene: OTOG

Linked Data

• dbSNP Id: rs1174973856
• gnomAD v3: 11-17642100-C-G
• gnomAD v4: 11-17642100-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17642100C>G , CM000673.2:g.17642100C>G	GRCh38
NC_000011.9:g.17663647C>G , CM000673.1:g.17663647C>G	GRCh37
NC_000011.8:g.17620223C>G	NCBI36
NG_033191.1:g.99728C>G
NG_033191.2:g.99728C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.8332-27C>G	ENSP00000382323.2:n.8332-27C>G
ENST00000399397.6:c.8296-27C>G MANE Select	ENSP00000382329.2:n.8296-27C>G
ENST00000399391.6:c.8332-27C>G	ENSP00000382323.2:n.8332-27C>G
ENST00000399397.5:c.8296-27C>G	ENSP00000382329.2:n.8296-27C>G
NM_001277269.1:c.8332-27C>G	NP_001264198.1:n.8332-27C>G
NM_001292063.1:c.8296-27C>G	NP_001278992.1:n.8296-27C>G
NM_001277269.2:c.8332-27C>G	NP_001264198.1:n.8332-27C>G
NM_001292063.2:c.8296-27C>G MANE Select	NP_001278992.1:n.8296-27C>G