Canonical Allele Identifier: CA2802149050
Gene: VSX2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259799del , CM000676.2:g.74259799del GRCh38
NC_000014.8:g.74726502del , CM000676.1:g.74726502del GRCh37
NC_000014.7:g.73796255del NCBI36
NG_013092.1:g.25328del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.760+17del MANE Select ENSP00000261980.2:n.760+17del
ENST00000261980.2:c.760+17del ENSP00000261980.2:n.760+17del
NM_182894.2:c.760+17del NP_878314.1:n.760+17del
XM_011536719.1:c.760+17del XP_011535021.1:n.760+17del
NM_182894.3:c.760+17del MANE Select NP_878314.1:n.760+17del
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