Canonical Allele Identifier: CA2396906838

Gene: PPIL2

Linked Data

• dbSNP Id: rs2066219604

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658390dup , CM000684.2:g.21658390dup	GRCh38
NC_000022.10:g.22012679dup , CM000684.1:g.22012679dup	GRCh37
NC_000022.9:g.20342679dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.286+1dup
ENST00000498589.1:n.467dup
XM_017029165.1:c.602dup	XP_016884654.1:p.Glu202ArgfsTer15
NR_169729.1:n.1202dup
NR_169730.1:n.1105dup
NR_169731.1:n.432-2447dup
NR_169732.1:n.256dup
NR_169733.1:n.314dup
NR_169734.1:n.338dup