Canonical Allele Identifier: CA2146964540
Gene: VSX2 HGNC NCBI

Linked Data

dbSNP Id: rs1594758855
gnomAD v4: 14-74259795-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74259795A>C , CM000676.2:g.74259795A>C GRCh38
NC_000014.8:g.74726498A>C , CM000676.1:g.74726498A>C GRCh37
NC_000014.7:g.73796251A>C NCBI36
NG_013092.1:g.25324A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261980.3:c.760+13A>C MANE Select ENSP00000261980.2:n.760+13A>C
ENST00000261980.2:c.760+13A>C ENSP00000261980.2:n.760+13A>C
NM_182894.2:c.760+13A>C NP_878314.1:n.760+13A>C
XM_011536719.1:c.760+13A>C XP_011535021.1:n.760+13A>C
NM_182894.3:c.760+13A>C MANE Select NP_878314.1:n.760+13A>C
Search 100 bp 5'
Search 100 bp 3'