Canonical Allele Identifier: CA18910159

Gene: OTUD3

Linked Data

• dbSNP Id: rs4654925
• gnomAD v2: 1-20227723-G-T
• gnomAD v3: 1-19901230-G-T
• gnomAD v4: 1-19901230-G-T
• MyVariant Identifiers: chr1:g.20227723G>T (hg19) ; chr1:g.19901230G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19901230G>T , CM000663.2:g.19901230G>T	GRCh38
NC_000001.10:g.20227723G>T , CM000663.1:g.20227723G>T	GRCh37
NC_000001.9:g.20100310G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375120.4:c.607-3037G>T MANE Select	ENSP00000364261.3:n.607-3037G>T
ENST00000375120.3:c.607-3037G>T	ENSP00000364261.3:n.607-3037G>T
NM_015207.1:c.607-3037G>T	NP_056022.1:n.607-3037G>T
XM_005245792.2:c.832-3037G>T	XP_005245849.1:n.832-3037G>T
XM_005245793.2:c.832-3037G>T	XP_005245850.1:n.832-3037G>T
XM_005245794.2:c.148-3037G>T	XP_005245851.1:n.148-3037G>T
XM_011541071.1:c.424-3037G>T	XP_011539373.1:n.424-3037G>T
XM_011541072.1:c.301-3037G>T	XP_011539374.1:n.301-3037G>T
XM_011541073.1:c.301-3037G>T	XP_011539375.1:n.301-3037G>T
XM_005245792.4:c.832-3037G>T	XP_005245849.1:n.832-3037G>T
XM_005245793.4:c.832-3037G>T	XP_005245850.1:n.832-3037G>T
XM_005245794.3:c.148-3037G>T	XP_005245851.1:n.148-3037G>T
XM_024454320.1:c.301-3037G>T	XP_024310088.1:n.301-3037G>T
NM_015207.2:c.607-3037G>T MANE Select	NP_056022.1:n.607-3037G>T