Canonical Allele Identifier: CA2612681883
Gene: OTOG HGNC NCBI

Linked Data

gnomAD v4: 11-17570135-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17570135G>C , CM000673.2:g.17570135G>C GRCh38
NC_000011.9:g.17591682G>C , CM000673.1:g.17591682G>C GRCh37
NC_000011.8:g.17548258G>C NCBI36
NG_033191.1:g.27763G>C
NG_033191.2:g.27763G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.1814-78G>C ENSP00000382323.2:n.1814-78G>C
ENST00000399397.6:c.1778-78G>C MANE Select ENSP00000382329.2:n.1778-78G>C
ENST00000399391.6:c.1814-78G>C ENSP00000382323.2:n.1814-78G>C
ENST00000399397.5:c.1778-78G>C ENSP00000382329.2:n.1778-78G>C
ENST00000498332.5:n.1684-78G>C
NM_001277269.1:c.1814-78G>C NP_001264198.1:n.1814-78G>C
NM_001292063.1:c.1778-78G>C NP_001278992.1:n.1778-78G>C
NM_001277269.2:c.1814-78G>C NP_001264198.1:n.1814-78G>C
NM_001292063.2:c.1778-78G>C MANE Select NP_001278992.1:n.1778-78G>C
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