Canonical Allele Identifier: CA708456151
Gene: VSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1209977437
MyVariant Identifiers: chr14:g.74726484del (hg19) chr14:g.74259781del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259783del , CM000676.2:g.74259783del GRCh38
NC_000014.8:g.74726486del , CM000676.1:g.74726486del GRCh37
NC_000014.7:g.73796239del NCBI36
NG_013092.1:g.25312del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.760+1del
ENST00000261980.2:c.760+1del
NM_182894.2:c.760+1del
XM_011536719.1:c.760+1del
NM_182894.3:c.760+1del
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