Canonical Allele Identifier: CA473301216
Gene: OTOG HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.17667407T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17645860T>A , CM000673.2:g.17645860T>A GRCh38
NC_000011.9:g.17667407T>A , CM000673.1:g.17667407T>A GRCh37
NC_000011.8:g.17623983T>A NCBI36
NG_033191.1:g.103488T>A
NG_033191.2:g.103488T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.8694T>A ENSP00000382323.2:p.Ser2898=
ENST00000399397.6:c.8658T>A MANE Select ENSP00000382329.2:p.Ser2886=
ENST00000399391.6:c.8694T>A ENSP00000382323.2:p.Ser2898=
ENST00000399397.5:c.8658T>A ENSP00000382329.2:p.Ser2886=
NM_001277269.1:c.8694T>A NP_001264198.1:p.Ser2898=
NM_001292063.1:c.8658T>A NP_001278992.1:p.Ser2886=
NM_001277269.2:c.8694T>A NP_001264198.1:p.Ser2898=
NM_001292063.2:c.8658T>A MANE Select NP_001278992.1:p.Ser2886=
Search 100 bp 5'
Search 100 bp 3'