Canonical Allele Identifier: CA582198230
Gene: TOX HGNC NCBI

Linked Data

dbSNP Id: rs1448092960
gnomAD v2: 8-59881133-C-A
gnomAD v3: 8-58968574-C-A
gnomAD v4: 8-58968574-C-A
MyVariant Identifiers: chr8:g.59881133C>A (hg19) chr8:g.58968574C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.58968574C>A , CM000670.2:g.58968574C>A GRCh38
NC_000008.10:g.59881133C>A , CM000670.1:g.59881133C>A GRCh37
NC_000008.9:g.60043687C>A NCBI36
NG_011993.1:g.155635G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361421.2:c.103-8566G>T MANE Select ENSP00000354842.1:n.103-8566G>T
ENST00000361421.1:c.103-8566G>T ENSP00000354842.1:n.103-8566G>T
NM_014729.2:c.103-8566G>T NP_055544.1:n.103-8566G>T
XM_017014085.1:c.103-29030G>T XP_016869574.1:n.103-29030G>T
NM_014729.3:c.103-8566G>T MANE Select NP_055544.1:n.103-8566G>T
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