Canonical Allele Identifier: CA177971386

Gene: TOX

Linked Data

• dbSNP Id: rs1001755479
• gnomAD v2: 8-59881098-G-A
• gnomAD v3: 8-58968539-G-A
• gnomAD v4: 8-58968539-G-A
• MyVariant Identifiers: chr8:g.59881098G>A (hg19) ; chr8:g.58968539G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.58968539G>A , CM000670.2:g.58968539G>A	GRCh38
NC_000008.10:g.59881098G>A , CM000670.1:g.59881098G>A	GRCh37
NC_000008.9:g.60043652G>A	NCBI36
NG_011993.1:g.155670C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361421.2:c.103-8531C>T MANE Select	ENSP00000354842.1:n.103-8531C>T
ENST00000361421.1:c.103-8531C>T	ENSP00000354842.1:n.103-8531C>T
NM_014729.2:c.103-8531C>T	NP_055544.1:n.103-8531C>T
XM_017014085.1:c.103-28995C>T	XP_016869574.1:n.103-28995C>T
NM_014729.3:c.103-8531C>T MANE Select	NP_055544.1:n.103-8531C>T