Canonical Allele Identifier: CA674260994

Gene: OTOG

Linked Data

• dbSNP Id: rs1252306090
• gnomAD v3: 11-17642094-A-T
• gnomAD v4: 11-17642094-A-T
• MyVariant Identifiers: chr11:g.17663641A>T (hg19) ; chr11:g.17642094A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17642094A>T , CM000673.2:g.17642094A>T	GRCh38
NC_000011.9:g.17663641A>T , CM000673.1:g.17663641A>T	GRCh37
NC_000011.8:g.17620217A>T	NCBI36
NG_033191.1:g.99722A>T
NG_033191.2:g.99722A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.8332-33A>T	ENSP00000382323.2:n.8332-33A>T
ENST00000399397.6:c.8296-33A>T MANE Select	ENSP00000382329.2:n.8296-33A>T
ENST00000399391.6:c.8332-33A>T	ENSP00000382323.2:n.8332-33A>T
ENST00000399397.5:c.8296-33A>T	ENSP00000382329.2:n.8296-33A>T
NM_001277269.1:c.8332-33A>T	NP_001264198.1:n.8332-33A>T
NM_001292063.1:c.8296-33A>T	NP_001278992.1:n.8296-33A>T
NM_001277269.2:c.8332-33A>T	NP_001264198.1:n.8332-33A>T
NM_001292063.2:c.8296-33A>T MANE Select	NP_001278992.1:n.8296-33A>T