Canonical Allele Identifier: CA1564718

Gene: OTOF

Linked Data

• dbSNP Id: rs766844731
• ExAC: 2:26741869 C / T
• gnomAD v2: 2-26741869-C-T
• gnomAD v4: 2-26519001-C-T
• MyVariant Identifiers: chr2:g.26741869C>T (hg19) ; chr2:g.26519001C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26519001C>T , CM000664.2:g.26519001C>T	GRCh38
NC_000002.11:g.26741869C>T , CM000664.1:g.26741869C>T	GRCh37
NC_000002.10:g.26595373C>T	NCBI36
NG_009937.1:g.44698G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.327+9G>A MANE Select	ENSP00000272371.2:n.327+9G>A
ENST00000272371.6:c.327+9G>A	ENSP00000272371.2:n.327+9G>A
ENST00000403946.7:c.327+9G>A	ENSP00000385255.3:n.327+9G>A
NM_001287489.1:c.327+9G>A	NP_001274418.1:n.327+9G>A
NM_194248.2:c.327+9G>A	NP_919224.1:n.327+9G>A
XM_005264644.2:c.327+9G>A	XP_005264701.1:n.327+9G>A
XM_011533185.1:c.327+9G>A	XP_011531487.1:n.327+9G>A
XM_017005338.1:c.327+9G>A	XP_016860827.1:n.327+9G>A
NM_001287489.2:c.327+9G>A	NP_001274418.1:n.327+9G>A
NM_194248.3:c.327+9G>A MANE Select	NP_919224.1:n.327+9G>A