Canonical Allele Identifier: CA473300342
Gene: OTOG HGNC NCBI

Linked Data

gnomAD v4: 11-17642231-G-A
MyVariant Identifiers: chr11:g.17663778G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17642231G>A , CM000673.2:g.17642231G>A GRCh38
NC_000011.9:g.17663778G>A , CM000673.1:g.17663778G>A GRCh37
NC_000011.8:g.17620354G>A NCBI36
NG_033191.1:g.99859G>A
NG_033191.2:g.99859G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.8436G>A ENSP00000382323.2:p.Glu2812=
ENST00000399397.6:c.8400G>A MANE Select ENSP00000382329.2:p.Glu2800=
ENST00000399391.6:c.8436G>A ENSP00000382323.2:p.Glu2812=
ENST00000399397.5:c.8400G>A ENSP00000382329.2:p.Glu2800=
NM_001277269.1:c.8436G>A NP_001264198.1:p.Glu2812=
NM_001292063.1:c.8400G>A NP_001278992.1:p.Glu2800=
NM_001277269.2:c.8436G>A NP_001264198.1:p.Glu2812=
NM_001292063.2:c.8400G>A MANE Select NP_001278992.1:p.Glu2800=
Search 100 bp 5'
Search 100 bp 3'