Canonical Allele Identifier: CA15968830
Gene: TOX2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.43945182C>A , CM000682.2:g.43945182C>A GRCh38
NC_000020.10:g.42573822C>A , CM000682.1:g.42573822C>A GRCh37
NC_000020.9:g.42007236C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000341197.9:c.100-28185C>A MANE Select ENSP00000344724.3:n.100-28185C>A
ENST00000341197.8:c.100-28185C>A ENSP00000344724.3:n.100-28185C>A
ENST00000372999.5:c.-152-9966C>A ENSP00000362090.1:n.-152-9966C>A
ENST00000423191.6:c.-27-28185C>A ENSP00000390278.1:n.-27-28185C>A
NM_001098796.1:c.-27-28185C>A NP_001092266.1:n.-27-28185C>A
NM_001098797.1:c.100-28185C>A NP_001092267.1:n.100-28185C>A
NM_032883.2:c.-152-9966C>A NP_116272.1:n.-152-9966C>A
NM_001098797.2:c.100-28185C>A MANE Select NP_001092267.1:n.100-28185C>A
NM_001098796.2:c.-27-28185C>A NP_001092266.1:n.-27-28185C>A
NM_032883.3:c.-152-9966C>A NP_116272.1:n.-152-9966C>A
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