Canonical Allele Identifier: CA2396906886

Gene: PPIL2

Linked Data

• dbSNP Id: rs2066220843

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658509G>T , CM000684.2:g.21658509G>T	GRCh38
NC_000022.10:g.22012798G>T , CM000684.1:g.22012798G>T	GRCh37
NC_000022.9:g.20342798G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000641967.1:n.286+120G>T
ENST00000498589.1:n.539+47G>T
XM_017029165.1:c.674+47G>T	XP_016884654.1:n.674+47G>T
NR_169729.1:n.1321G>T
NR_169730.1:n.1224G>T
NR_169731.1:n.432-2328G>T
NR_169732.1:n.328+47G>T
NR_169733.1:n.386+47G>T
NR_169734.1:n.410+47G>T