Canonical Allele Identifier: CA12853862
Gene: TOX HGNC NCBI

Linked Data

dbSNP Id: rs11777927
gnomAD v2: 8-59881039-A-T
gnomAD v3: 8-58968480-A-T
gnomAD v4: 8-58968480-A-T
MyVariant Identifiers: chr8:g.59881039A>T (hg19) chr8:g.58968480A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.58968480A>T , CM000670.2:g.58968480A>T GRCh38
NC_000008.10:g.59881039A>T , CM000670.1:g.59881039A>T GRCh37
NC_000008.9:g.60043593A>T NCBI36
NG_011993.1:g.155729T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361421.2:c.103-8472T>A MANE Select ENSP00000354842.1:n.103-8472T>A
ENST00000361421.1:c.103-8472T>A ENSP00000354842.1:n.103-8472T>A
NM_014729.2:c.103-8472T>A NP_055544.1:n.103-8472T>A
XM_017014085.1:c.103-28936T>A XP_016869574.1:n.103-28936T>A
NM_014729.3:c.103-8472T>A MANE Select NP_055544.1:n.103-8472T>A
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