Canonical Allele Identifier: CA513535663

Gene: PPIL2

Linked Data

• gnomAD v4: 22-21658453-C-A
• MyVariant Identifiers: chr22:g.22012742C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658453C>A , CM000684.2:g.21658453C>A	GRCh38
NC_000022.10:g.22012742C>A , CM000684.1:g.22012742C>A	GRCh37
NC_000022.9:g.20342742C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.286+64C>A
ENST00000498589.1:n.530C>A
XM_017029165.1:c.665C>A	XP_016884654.1:p.Pro222Gln
NR_169729.1:n.1265C>A
NR_169730.1:n.1168C>A
NR_169731.1:n.432-2384C>A
NR_169732.1:n.319C>A
NR_169733.1:n.377C>A
NR_169734.1:n.401C>A