Canonical Allele Identifier: CA281874294

Gene: TOX3

Linked Data

• dbSNP Id: rs1001373150
• gnomAD v2: 16-52576120-C-T
• gnomAD v3: 16-52542208-C-T
• gnomAD v4: 16-52542208-C-T
• MyVariant Identifiers: chr16:g.52576120C>T (hg19) ; chr16:g.52542208C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.52542208C>T , CM000678.2:g.52542208C>T	GRCh38
NC_000016.9:g.52576120C>T , CM000678.1:g.52576120C>T	GRCh37
NC_000016.8:g.51133621C>T	NCBI36
NG_012623.1:g.10595G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219746.14:c.87+4429G>A MANE Select	ENSP00000219746.9:n.87+4429G>A
ENST00000219746.13:c.87+4429G>A	ENSP00000219746.9:n.87+4429G>A
ENST00000407228.7:c.-100+5506G>A	ENSP00000385705.3:n.-100+5506G>A
ENST00000563091.1:c.-22+5160G>A	ENSP00000457401.1:n.-22+5160G>A
ENST00000568436.1:c.87+4429G>A	ENSP00000463843.1:n.87+4429G>A
NM_001080430.2:c.87+4429G>A	NP_001073899.2:n.87+4429G>A
NM_001146188.1:c.-100+5506G>A	NP_001139660.1:n.-100+5506G>A
XM_005255892.2:c.87+4429G>A	XP_005255949.1:n.87+4429G>A
XM_005255893.2:c.-100+4429G>A	XP_005255950.1:n.-100+4429G>A
NM_001080430.3:c.87+4429G>A	NP_001073899.2:n.87+4429G>A
NM_001146188.2:c.-100+5506G>A	NP_001139660.1:n.-100+5506G>A
XM_005255892.3:c.87+4429G>A	XP_005255949.1:n.87+4429G>A
NM_001080430.4:c.87+4429G>A MANE Select	NP_001073899.2:n.87+4429G>A