Canonical Allele Identifier: CA1787195445
Gene: TOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.58968501G= , CM000670.2:g.58968501G= GRCh38
NC_000008.10:g.59881060G= , CM000670.1:g.59881060G= GRCh37
NC_000008.9:g.60043614G= NCBI36
NG_011993.1:g.155708C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361421.2:c.103-8493C= MANE Select ENSP00000354842.1:n.103-8493C=
ENST00000361421.1:c.103-8493C= ENSP00000354842.1:n.103-8493C=
NM_014729.2:c.103-8493C= NP_055544.1:n.103-8493C=
XM_017014085.1:c.103-28957C= XP_016869574.1:n.103-28957C=
NM_014729.3:c.103-8493C= MANE Select NP_055544.1:n.103-8493C=