Canonical Allele Identifier: CA513535256

Gene: PPIL2

Linked Data

• dbSNP Id: rs1247890590
• gnomAD v4: 22-21658326-G-A
• MyVariant Identifiers: chr22:g.22012615G>A (hg19) ; chr22:g.21658326G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658326G>A , CM000684.2:g.21658326G>A	GRCh38
NC_000022.10:g.22012615G>A , CM000684.1:g.22012615G>A	GRCh37
NC_000022.9:g.20342615G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.223G>A
ENST00000498589.1:n.403G>A
XM_017029165.1:c.538G>A	XP_016884654.1:p.Glu180Lys
NR_169729.1:n.1138G>A
NR_169730.1:n.1041G>A
NR_169731.1:n.432-2511G>A
NR_169732.1:n.192G>A
NR_169733.1:n.250G>A
NR_169734.1:n.274G>A