Canonical Allele Identifier: CA597905175

Gene: OTOG

Linked Data

• dbSNP Id: rs1299780033
• gnomAD v2: 11-17663659-T-C
• gnomAD v4: 11-17642112-T-C
• MyVariant Identifiers: chr11:g.17663659T>C (hg19) ; chr11:g.17642112T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17642112T>C , CM000673.2:g.17642112T>C	GRCh38
NC_000011.9:g.17663659T>C , CM000673.1:g.17663659T>C	GRCh37
NC_000011.8:g.17620235T>C	NCBI36
NG_033191.1:g.99740T>C
NG_033191.2:g.99740T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.8332-15T>C	ENSP00000382323.2:n.8332-15T>C
ENST00000399397.6:c.8296-15T>C MANE Select	ENSP00000382329.2:n.8296-15T>C
ENST00000399391.6:c.8332-15T>C	ENSP00000382323.2:n.8332-15T>C
ENST00000399397.5:c.8296-15T>C	ENSP00000382329.2:n.8296-15T>C
NM_001277269.1:c.8332-15T>C	NP_001264198.1:n.8332-15T>C
NM_001292063.1:c.8296-15T>C	NP_001278992.1:n.8296-15T>C
NM_001277269.2:c.8332-15T>C	NP_001264198.1:n.8332-15T>C
NM_001292063.2:c.8296-15T>C MANE Select	NP_001278992.1:n.8296-15T>C