Canonical Allele Identifier: CA1787195498
Gene: TOX HGNC NCBI

Linked Data

dbSNP Id: rs1812944976
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.58968566A>T , CM000670.2:g.58968566A>T GRCh38
NC_000008.10:g.59881125A>T , CM000670.1:g.59881125A>T GRCh37
NC_000008.9:g.60043679A>T NCBI36
NG_011993.1:g.155643T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361421.2:c.103-8558T>A MANE Select ENSP00000354842.1:n.103-8558T>A
ENST00000361421.1:c.103-8558T>A ENSP00000354842.1:n.103-8558T>A
NM_014729.2:c.103-8558T>A NP_055544.1:n.103-8558T>A
XM_017014085.1:c.103-29022T>A XP_016869574.1:n.103-29022T>A
NM_014729.3:c.103-8558T>A MANE Select NP_055544.1:n.103-8558T>A
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