Canonical Allele Identifier: CA281871034

Gene: TOX3

Linked Data

• dbSNP Id: rs552569672
• gnomAD v2: 16-52548018-A-T
• gnomAD v3: 16-52514106-A-T
• gnomAD v4: 16-52514106-A-T
• MyVariant Identifiers: chr16:g.52548018A>T (hg19) ; chr16:g.52514106A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.52514106A>T , CM000678.2:g.52514106A>T	GRCh38
NC_000016.9:g.52548018A>T , CM000678.1:g.52548018A>T	GRCh37
NC_000016.8:g.51105519A>T	NCBI36
NG_012623.1:g.38697T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219746.14:c.87+32531T>A MANE Select	ENSP00000219746.9:n.87+32531T>A
ENST00000219746.13:c.87+32531T>A	ENSP00000219746.9:n.87+32531T>A
ENST00000407228.7:c.75+5300T>A	ENSP00000385705.3:n.75+5300T>A
ENST00000563091.1:c.-22+33262T>A	ENSP00000457401.1:n.-22+33262T>A
ENST00000568436.1:c.87+32531T>A	ENSP00000463843.1:n.87+32531T>A
NM_001080430.2:c.87+32531T>A	NP_001073899.2:n.87+32531T>A
NM_001146188.1:c.75+5300T>A	NP_001139660.1:n.75+5300T>A
XM_005255892.2:c.87+32531T>A	XP_005255949.1:n.87+32531T>A
XM_005255893.2:c.75+5300T>A	XP_005255950.1:n.75+5300T>A
NM_001080430.3:c.87+32531T>A	NP_001073899.2:n.87+32531T>A
NM_001146188.2:c.75+5300T>A	NP_001139660.1:n.75+5300T>A
XM_005255892.3:c.87+32531T>A	XP_005255949.1:n.87+32531T>A
XM_017023142.1:c.75+5300T>A	XP_016878631.1:n.75+5300T>A
XM_024450230.1:c.75+5300T>A	XP_024305998.1:n.75+5300T>A
NM_001080430.4:c.87+32531T>A MANE Select	NP_001073899.2:n.87+32531T>A