Canonical Allele Identifier: CA513535162

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012581G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658292G>A , CM000684.2:g.21658292G>A	GRCh38
NC_000022.10:g.22012581G>A , CM000684.1:g.22012581G>A	GRCh37
NC_000022.9:g.20342581G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.189G>A
ENST00000498589.1:n.369G>A
XM_017029165.1:c.504G>A	XP_016884654.1:p.Ala168=
NR_169729.1:n.1104G>A
NR_169730.1:n.1007G>A
NR_169731.1:n.432-2545G>A
NR_169732.1:n.158G>A
NR_169733.1:n.216G>A
NR_169734.1:n.240G>A