Canonical Allele Identifier: CA767289416

Gene: OTOF

Linked Data

• dbSNP Id: rs1229884928
• gnomAD v3: 2-26482244-A-C
• gnomAD v4: 2-26482244-A-C
• MyVariant Identifiers: chr2:g.26705112A>C (hg19) ; chr2:g.26482244A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482244A>C , CM000664.2:g.26482244A>C	GRCh38
NC_000002.11:g.26705112A>C , CM000664.1:g.26705112A>C	GRCh37
NC_000002.10:g.26558616A>C	NCBI36
NG_009937.1:g.81455T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1579+162T>G MANE Select	ENSP00000272371.2:n.1579+162T>G
ENST00000272371.6:c.1579+162T>G	ENSP00000272371.2:n.1579+162T>G
ENST00000403946.7:c.1579+162T>G	ENSP00000385255.3:n.1579+162T>G
NM_001287489.1:c.1579+162T>G	NP_001274418.1:n.1579+162T>G
NM_194248.2:c.1579+162T>G	NP_919224.1:n.1579+162T>G
XM_005264644.2:c.1624+162T>G	XP_005264701.1:n.1624+162T>G
XM_011533185.1:c.1624+162T>G	XP_011531487.1:n.1624+162T>G
XM_017005338.1:c.1579+162T>G	XP_016860827.1:n.1579+162T>G
NM_001287489.2:c.1579+162T>G	NP_001274418.1:n.1579+162T>G
NM_194248.3:c.1579+162T>G MANE Select	NP_919224.1:n.1579+162T>G