Canonical Allele Identifier: CA1787195356
Gene: TOX HGNC NCBI

Linked Data

dbSNP Id: rs1812942265
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.58968426_58968427del , CM000670.2:g.58968426_58968427del GRCh38
NC_000008.10:g.59880985_59880986del , CM000670.1:g.59880985_59880986del GRCh37
NC_000008.9:g.60043539_60043540del NCBI36
NG_011993.1:g.155784_155785del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361421.2:c.103-8417_103-8416del MANE Select ENSP00000354842.1:n.103-8417_103-8416del
ENST00000361421.1:c.103-8417_103-8416del ENSP00000354842.1:n.103-8417_103-8416del
NM_014729.2:c.103-8417_103-8416del NP_055544.1:n.103-8417_103-8416del
XM_017014085.1:c.103-28881_103-28880del XP_016869574.1:n.103-28881_103-28880del
NM_014729.3:c.103-8417_103-8416del MANE Select NP_055544.1:n.103-8417_103-8416del
Search 100 bp 5'
Search 100 bp 3'