Canonical Allele Identifier: CA853735983
Gene: TOX HGNC NCBI

Linked Data

dbSNP Id: rs1290353374
gnomAD v3: 8-58968433-A-G
gnomAD v4: 8-58968433-A-G
MyVariant Identifiers: chr8:g.59880992A>G (hg19) chr8:g.58968433A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.58968433A>G , CM000670.2:g.58968433A>G GRCh38
NC_000008.10:g.59880992A>G , CM000670.1:g.59880992A>G GRCh37
NC_000008.9:g.60043546A>G NCBI36
NG_011993.1:g.155776T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361421.2:c.103-8425T>C MANE Select ENSP00000354842.1:n.103-8425T>C
ENST00000361421.1:c.103-8425T>C ENSP00000354842.1:n.103-8425T>C
NM_014729.2:c.103-8425T>C NP_055544.1:n.103-8425T>C
XM_017014085.1:c.103-28889T>C XP_016869574.1:n.103-28889T>C
NM_014729.3:c.103-8425T>C MANE Select NP_055544.1:n.103-8425T>C
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