Canonical Allele Identifier: CA622534125

Gene: TOX3

Linked Data

• dbSNP Id: rs1393193805
• gnomAD v2: 16-52548417-T-C
• gnomAD v3: 16-52514505-T-C
• gnomAD v4: 16-52514505-T-C
• MyVariant Identifiers: chr16:g.52548417T>C (hg19) ; chr16:g.52514505T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.52514505T>C , CM000678.2:g.52514505T>C	GRCh38
NC_000016.9:g.52548417T>C , CM000678.1:g.52548417T>C	GRCh37
NC_000016.8:g.51105918T>C	NCBI36
NG_012623.1:g.38298A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219746.14:c.87+32132A>G MANE Select	ENSP00000219746.9:n.87+32132A>G
ENST00000219746.13:c.87+32132A>G	ENSP00000219746.9:n.87+32132A>G
ENST00000407228.7:c.75+4901A>G	ENSP00000385705.3:n.75+4901A>G
ENST00000563091.1:c.-22+32863A>G	ENSP00000457401.1:n.-22+32863A>G
ENST00000568436.1:c.87+32132A>G	ENSP00000463843.1:n.87+32132A>G
NM_001080430.2:c.87+32132A>G	NP_001073899.2:n.87+32132A>G
NM_001146188.1:c.75+4901A>G	NP_001139660.1:n.75+4901A>G
XM_005255892.2:c.87+32132A>G	XP_005255949.1:n.87+32132A>G
XM_005255893.2:c.75+4901A>G	XP_005255950.1:n.75+4901A>G
NM_001080430.3:c.87+32132A>G	NP_001073899.2:n.87+32132A>G
NM_001146188.2:c.75+4901A>G	NP_001139660.1:n.75+4901A>G
XM_005255892.3:c.87+32132A>G	XP_005255949.1:n.87+32132A>G
XM_017023142.1:c.75+4901A>G	XP_016878631.1:n.75+4901A>G
XM_024450230.1:c.75+4901A>G	XP_024305998.1:n.75+4901A>G
NM_001080430.4:c.87+32132A>G MANE Select	NP_001073899.2:n.87+32132A>G