Canonical Allele Identifier: CA2612681889
Gene: OTOG HGNC NCBI

Linked Data

gnomAD v4: 11-17570139-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17570139C>A , CM000673.2:g.17570139C>A GRCh38
NC_000011.9:g.17591686C>A , CM000673.1:g.17591686C>A GRCh37
NC_000011.8:g.17548262C>A NCBI36
NG_033191.1:g.27767C>A
NG_033191.2:g.27767C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.1814-74C>A ENSP00000382323.2:n.1814-74C>A
ENST00000399397.6:c.1778-74C>A MANE Select ENSP00000382329.2:n.1778-74C>A
ENST00000399391.6:c.1814-74C>A ENSP00000382323.2:n.1814-74C>A
ENST00000399397.5:c.1778-74C>A ENSP00000382329.2:n.1778-74C>A
ENST00000498332.5:n.1684-74C>A
NM_001277269.1:c.1814-74C>A NP_001264198.1:n.1814-74C>A
NM_001292063.1:c.1778-74C>A NP_001278992.1:n.1778-74C>A
NM_001277269.2:c.1814-74C>A NP_001264198.1:n.1814-74C>A
NM_001292063.2:c.1778-74C>A MANE Select NP_001278992.1:n.1778-74C>A
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