Canonical Allele Identifier: CA2612679111
Gene: OTOG HGNC NCBI

Linked Data

gnomAD v4: 11-17553023-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553023A>C , CM000673.2:g.17553023A>C GRCh38
NC_000011.9:g.17574570A>C , CM000673.1:g.17574570A>C GRCh37
NC_000011.8:g.17531146A>C NCBI36
NG_033191.1:g.10651A>C
NG_033191.2:g.10651A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.329-96A>C ENSP00000382323.2:n.329-96A>C
ENST00000399397.6:c.293-96A>C MANE Select ENSP00000382329.2:n.293-96A>C
ENST00000399391.6:c.329-96A>C ENSP00000382323.2:n.329-96A>C
ENST00000399397.5:c.293-96A>C ENSP00000382329.2:n.293-96A>C
ENST00000428619.1:c.110-96A>C ENSP00000399057.2:n.110-96A>C
ENST00000498332.5:n.199-96A>C
NM_001277269.1:c.329-96A>C NP_001264198.1:n.329-96A>C
NM_001292063.1:c.293-96A>C NP_001278992.1:n.293-96A>C
NM_001277269.2:c.329-96A>C NP_001264198.1:n.329-96A>C
NM_001292063.2:c.293-96A>C MANE Select NP_001278992.1:n.293-96A>C
Search 100 bp 5'
Search 100 bp 3'