Canonical Allele Identifier: CA2730029659

Gene: VSX2

Linked Data

• dbSNP Id: rs2139645784

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74259556dup , CM000676.2:g.74259556dup	GRCh38
NC_000014.8:g.74726259dup , CM000676.1:g.74726259dup	GRCh37
NC_000014.7:g.73796012dup	NCBI36
NG_013092.1:g.25085dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261980.3:c.580-46dup MANE Select	ENSP00000261980.2:n.580-46dup
ENST00000261980.2:c.580-46dup	ENSP00000261980.2:n.580-46dup
NM_182894.2:c.580-46dup	NP_878314.1:n.580-46dup
XM_011536719.1:c.580-46dup	XP_011535021.1:n.580-46dup
NM_182894.3:c.580-46dup MANE Select	NP_878314.1:n.580-46dup