Canonical Allele Identifier: CA1787195481
Gene: TOX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.58968562T= , CM000670.2:g.58968562T= GRCh38
NC_000008.10:g.59881121T= , CM000670.1:g.59881121T= GRCh37
NC_000008.9:g.60043675T= NCBI36
NG_011993.1:g.155647A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361421.2:c.103-8554A= MANE Select ENSP00000354842.1:n.103-8554A=
ENST00000361421.1:c.103-8554A= ENSP00000354842.1:n.103-8554A=
NM_014729.2:c.103-8554A= NP_055544.1:n.103-8554A=
XM_017014085.1:c.103-29018A= XP_016869574.1:n.103-29018A=
NM_014729.3:c.103-8554A= MANE Select NP_055544.1:n.103-8554A=
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