Canonical Allele Identifier: CA2612681895
Gene: OTOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17570143C>T , CM000673.2:g.17570143C>T GRCh38
NC_000011.9:g.17591690C>T , CM000673.1:g.17591690C>T GRCh37
NC_000011.8:g.17548266C>T NCBI36
NG_033191.1:g.27771C>T
NG_033191.2:g.27771C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.1814-70C>T ENSP00000382323.2:n.1814-70C>T
ENST00000399397.6:c.1778-70C>T MANE Select ENSP00000382329.2:n.1778-70C>T
ENST00000399391.6:c.1814-70C>T ENSP00000382323.2:n.1814-70C>T
ENST00000399397.5:c.1778-70C>T ENSP00000382329.2:n.1778-70C>T
ENST00000498332.5:n.1684-70C>T
NM_001277269.1:c.1814-70C>T NP_001264198.1:n.1814-70C>T
NM_001292063.1:c.1778-70C>T NP_001278992.1:n.1778-70C>T
NM_001277269.2:c.1814-70C>T NP_001264198.1:n.1814-70C>T
NM_001292063.2:c.1778-70C>T MANE Select NP_001278992.1:n.1778-70C>T