Canonical Allele Identifier: CA1787195419
Gene: TOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.58968486T= , CM000670.2:g.58968486T= GRCh38
NC_000008.10:g.59881045T= , CM000670.1:g.59881045T= GRCh37
NC_000008.9:g.60043599T= NCBI36
NG_011993.1:g.155723A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361421.2:c.103-8478A= MANE Select ENSP00000354842.1:n.103-8478A=
ENST00000361421.1:c.103-8478A= ENSP00000354842.1:n.103-8478A=
NM_014729.2:c.103-8478A= NP_055544.1:n.103-8478A=
XM_017014085.1:c.103-28942A= XP_016869574.1:n.103-28942A=
NM_014729.3:c.103-8478A= MANE Select NP_055544.1:n.103-8478A=