Canonical Allele Identifier: CA177971381

Gene: TOX

Linked Data

• dbSNP Id: rs1011039707
• MyVariant Identifiers: chr8:g.59881056C>G (hg19) ; chr8:g.58968497C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.58968497C>G , CM000670.2:g.58968497C>G	GRCh38
NC_000008.10:g.59881056C>G , CM000670.1:g.59881056C>G	GRCh37
NC_000008.9:g.60043610C>G	NCBI36
NG_011993.1:g.155712G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361421.2:c.103-8489G>C MANE Select	ENSP00000354842.1:n.103-8489G>C
ENST00000361421.1:c.103-8489G>C	ENSP00000354842.1:n.103-8489G>C
NM_014729.2:c.103-8489G>C	NP_055544.1:n.103-8489G>C
XM_017014085.1:c.103-28953G>C	XP_016869574.1:n.103-28953G>C
NM_014729.3:c.103-8489G>C MANE Select	NP_055544.1:n.103-8489G>C