Canonical Allele Identifier: CA597904770

Gene: OTOG

Linked Data

• dbSNP Id: rs1462401390
• gnomAD v2: 11-17574890-G-C
• gnomAD v4: 11-17553343-G-C
• MyVariant Identifiers: chr11:g.17574890G>C (hg19) ; chr11:g.17553343G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553343G>C , CM000673.2:g.17553343G>C	GRCh38
NC_000011.9:g.17574890G>C , CM000673.1:g.17574890G>C	GRCh37
NC_000011.8:g.17531466G>C	NCBI36
NG_033191.1:g.10971G>C
NG_033191.2:g.10971G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.422-22G>C	ENSP00000382323.2:n.422-22G>C
ENST00000399397.6:c.386-22G>C MANE Select	ENSP00000382329.2:n.386-22G>C
ENST00000399391.6:c.422-22G>C	ENSP00000382323.2:n.422-22G>C
ENST00000399397.5:c.386-22G>C	ENSP00000382329.2:n.386-22G>C
ENST00000428619.1:c.203-22G>C	ENSP00000399057.2:n.203-22G>C
ENST00000498332.5:n.292-22G>C
NM_001277269.1:c.422-22G>C	NP_001264198.1:n.422-22G>C
NM_001292063.1:c.386-22G>C	NP_001278992.1:n.386-22G>C
NM_001277269.2:c.422-22G>C	NP_001264198.1:n.422-22G>C
NM_001292063.2:c.386-22G>C MANE Select	NP_001278992.1:n.386-22G>C