Canonical Allele Identifier: CA322311182

Gene: PPIL2

Linked Data

• dbSNP Id: rs927081270
• MyVariant Identifiers: chr22:g.22012876T>G (hg19) ; chr22:g.21658587T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658587T>G , CM000684.2:g.21658587T>G	GRCh38
NC_000022.10:g.22012876T>G , CM000684.1:g.22012876T>G	GRCh37
NC_000022.9:g.20342876T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.286+198T>G
ENST00000498589.1:n.540-56T>G
XM_017029165.1:c.674+125T>G	XP_016884654.1:n.674+125T>G
NR_169729.1:n.1399T>G
NR_169730.1:n.1302T>G
NR_169731.1:n.432-2250T>G
NR_169732.1:n.328+125T>G
NR_169733.1:n.387-56T>G
NR_169734.1:n.411-56T>G