Canonical Allele Identifier: CA218479051

Gene: OTOG

Linked Data

• dbSNP Id: rs747688631
• gnomAD v3: 11-17612839-A-C
• gnomAD v4: 11-17612839-A-C
• MyVariant Identifiers: chr11:g.17634386A>C (hg19) ; chr11:g.17612839A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612839A>C , CM000673.2:g.17612839A>C	GRCh38
NC_000011.9:g.17634386A>C , CM000673.1:g.17634386A>C	GRCh37
NC_000011.8:g.17590962A>C	NCBI36
NG_033191.1:g.70467A>C
NG_033191.2:g.70467A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6474+74A>C	ENSP00000382323.2:n.6474+74A>C
ENST00000399397.6:c.6438+74A>C MANE Select	ENSP00000382329.2:n.6438+74A>C
ENST00000342528.2:c.3492+74A>C	ENSP00000341666.2:n.3492+74A>C
ENST00000399391.6:c.6474+74A>C	ENSP00000382323.2:n.6474+74A>C
ENST00000399397.5:c.6438+74A>C	ENSP00000382329.2:n.6438+74A>C
NM_001277269.1:c.6474+74A>C	NP_001264198.1:n.6474+74A>C
NM_001292063.1:c.6438+74A>C	NP_001278992.1:n.6438+74A>C
NM_001277269.2:c.6474+74A>C	NP_001264198.1:n.6474+74A>C
NM_001292063.2:c.6438+74A>C MANE Select	NP_001278992.1:n.6438+74A>C