Canonical Allele Identifier: CA177971373

Gene: TOX

Linked Data

• dbSNP Id: rs138292784
• gnomAD v2: 8-59880965-C-T
• gnomAD v3: 8-58968406-C-T
• gnomAD v4: 8-58968406-C-T
• MyVariant Identifiers: chr8:g.59880965C>T (hg19) ; chr8:g.58968406C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.58968406C>T , CM000670.2:g.58968406C>T	GRCh38
NC_000008.10:g.59880965C>T , CM000670.1:g.59880965C>T	GRCh37
NC_000008.9:g.60043519C>T	NCBI36
NG_011993.1:g.155803G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361421.2:c.103-8398G>A MANE Select	ENSP00000354842.1:n.103-8398G>A
ENST00000361421.1:c.103-8398G>A	ENSP00000354842.1:n.103-8398G>A
NM_014729.2:c.103-8398G>A	NP_055544.1:n.103-8398G>A
XM_017014085.1:c.103-28862G>A	XP_016869574.1:n.103-28862G>A
NM_014729.3:c.103-8398G>A MANE Select	NP_055544.1:n.103-8398G>A