Canonical Allele Identifier: CA2396906884

Gene: PPIL2

Linked Data

• dbSNP Id: rs2066220815

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658508G>A , CM000684.2:g.21658508G>A	GRCh38
NC_000022.10:g.22012797G>A , CM000684.1:g.22012797G>A	GRCh37
NC_000022.9:g.20342797G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000641967.1:n.286+119G>A
ENST00000498589.1:n.539+46G>A
XM_017029165.1:c.674+46G>A	XP_016884654.1:n.674+46G>A
NR_169729.1:n.1320G>A
NR_169730.1:n.1223G>A
NR_169731.1:n.432-2329G>A
NR_169732.1:n.328+46G>A
NR_169733.1:n.386+46G>A
NR_169734.1:n.410+46G>A