Canonical Allele Identifier: CA473516788
Gene: OTOG HGNC NCBI

Linked Data

gnomAD v4: 11-17553474-C-A
MyVariant Identifiers: chr11:g.17575021C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553474C>A , CM000673.2:g.17553474C>A GRCh38
NC_000011.9:g.17575021C>A , CM000673.1:g.17575021C>A GRCh37
NC_000011.8:g.17531597C>A NCBI36
NG_033191.1:g.11102C>A
NG_033191.2:g.11102C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.531C>A ENSP00000382323.2:p.Thr177=
ENST00000399397.6:c.495C>A MANE Select ENSP00000382329.2:p.Thr165=
ENST00000399391.6:c.531C>A ENSP00000382323.2:p.Thr177=
ENST00000399397.5:c.495C>A ENSP00000382329.2:p.Thr165=
ENST00000498332.5:n.401C>A
NM_001277269.1:c.531C>A NP_001264198.1:p.Thr177=
NM_001292063.1:c.495C>A NP_001278992.1:p.Thr165=
NM_001277269.2:c.531C>A NP_001264198.1:p.Thr177=
NM_001292063.2:c.495C>A MANE Select NP_001278992.1:p.Thr165=
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