Canonical Allele Identifier: CA513535177

Gene: PPIL2

Linked Data

• gnomAD v4: 22-21658298-G-T
• MyVariant Identifiers: chr22:g.22012587G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658298G>T , CM000684.2:g.21658298G>T	GRCh38
NC_000022.10:g.22012587G>T , CM000684.1:g.22012587G>T	GRCh37
NC_000022.9:g.20342587G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.195G>T
ENST00000498589.1:n.375G>T
XM_017029165.1:c.510G>T	XP_016884654.1:p.Leu170=
NR_169729.1:n.1110G>T
NR_169730.1:n.1013G>T
NR_169731.1:n.432-2539G>T
NR_169732.1:n.164G>T
NR_169733.1:n.222G>T
NR_169734.1:n.246G>T