Canonical Allele Identifier: CA177971370

Gene: TOX

Linked Data

• dbSNP Id: rs75438882
• gnomAD v2: 8-59880958-A-G
• gnomAD v3: 8-58968399-A-G
• gnomAD v4: 8-58968399-A-G
• MyVariant Identifiers: chr8:g.59880958A>G (hg19) ; chr8:g.58968399A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.58968399A>G , CM000670.2:g.58968399A>G	GRCh38
NC_000008.10:g.59880958A>G , CM000670.1:g.59880958A>G	GRCh37
NC_000008.9:g.60043512A>G	NCBI36
NG_011993.1:g.155810T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361421.2:c.103-8391T>C MANE Select	ENSP00000354842.1:n.103-8391T>C
ENST00000361421.1:c.103-8391T>C	ENSP00000354842.1:n.103-8391T>C
NM_014729.2:c.103-8391T>C	NP_055544.1:n.103-8391T>C
XM_017014085.1:c.103-28855T>C	XP_016869574.1:n.103-28855T>C
NM_014729.3:c.103-8391T>C MANE Select	NP_055544.1:n.103-8391T>C