Canonical Allele Identifier: CA1955197902

Gene: OTOG

Linked Data

• dbSNP Id: rs1851996034

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553696C>G , CM000673.2:g.17553696C>G	GRCh38
NC_000011.9:g.17575243C>G , CM000673.1:g.17575243C>G	GRCh37
NC_000011.8:g.17531819C>G	NCBI36
NG_033191.1:g.11324C>G
NG_033191.2:g.11324C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.576+177C>G	ENSP00000382323.2:n.576+177C>G
ENST00000399397.6:c.540+177C>G MANE Select	ENSP00000382329.2:n.540+177C>G
ENST00000399391.6:c.576+177C>G	ENSP00000382323.2:n.576+177C>G
ENST00000399397.5:c.540+177C>G	ENSP00000382329.2:n.540+177C>G
ENST00000498332.5:n.446+177C>G
NM_001277269.1:c.576+177C>G	NP_001264198.1:n.576+177C>G
NM_001292063.1:c.540+177C>G	NP_001278992.1:n.540+177C>G
NM_001277269.2:c.576+177C>G	NP_001264198.1:n.576+177C>G
NM_001292063.2:c.540+177C>G MANE Select	NP_001278992.1:n.540+177C>G