Canonical Allele Identifier: CA263556740

Gene: VSX2

Linked Data

• dbSNP Id: rs375150332
• MyVariant Identifiers: chr14:g.74726486G>A (hg19) ; chr14:g.74259783G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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