Canonical Allele Identifier: CA2695219547
Gene: VSX2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2764044
ClinVar RCV Id: RCV003517658
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259656del , CM000676.2:g.74259656del GRCh38
NC_000014.8:g.74726359del , CM000676.1:g.74726359del GRCh37
NC_000014.7:g.73796112del NCBI36
NG_013092.1:g.25185del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.634del MANE Select ENSP00000261980.2:p.Arg212GlyfsTer?
ENST00000261980.2:c.634del ENSP00000261980.2:p.Arg212GlyfsTer?
NM_182894.2:c.634del NP_878314.1:p.Arg212GlyfsTer?
XM_011536719.1:c.634del XP_011535021.1:p.Arg212GlyfsTer?
NM_182894.3:c.634del MANE Select NP_878314.1:p.Arg212GlyfsTer?
Search 100 bp 5'
Search 100 bp 3'