Canonical Allele Identifier: CA2612690020
Gene: OTOG HGNC NCBI

Linked Data

gnomAD v4: 11-17635017-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17635017C>A , CM000673.2:g.17635017C>A GRCh38
NC_000011.9:g.17656564C>A , CM000673.1:g.17656564C>A GRCh37
NC_000011.8:g.17613140C>A NCBI36
NG_033191.1:g.92645C>A
NG_033191.2:g.92645C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.7622-63C>A ENSP00000382323.2:n.7622-63C>A
ENST00000399397.6:c.7586-63C>A MANE Select ENSP00000382329.2:n.7586-63C>A
ENST00000342528.2:c.4322-593C>A ENSP00000341666.2:n.4322-593C>A
ENST00000399391.6:c.7622-63C>A ENSP00000382323.2:n.7622-63C>A
ENST00000399397.5:c.7586-63C>A ENSP00000382329.2:n.7586-63C>A
NM_001277269.1:c.7622-63C>A NP_001264198.1:n.7622-63C>A
NM_001292063.1:c.7586-63C>A NP_001278992.1:n.7586-63C>A
NM_001277269.2:c.7622-63C>A NP_001264198.1:n.7622-63C>A
NM_001292063.2:c.7586-63C>A MANE Select NP_001278992.1:n.7586-63C>A
Search 100 bp 5'
Search 100 bp 3'