Canonical Allele Identifier: CA2655514840

Gene: PPIL2

Linked Data

• gnomAD v4: 22-21658490-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658490T>A , CM000684.2:g.21658490T>A	GRCh38
NC_000022.10:g.22012779T>A , CM000684.1:g.22012779T>A	GRCh37
NC_000022.9:g.20342779T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000641967.1:n.286+101T>A
ENST00000498589.1:n.539+28T>A
XM_017029165.1:c.674+28T>A	XP_016884654.1:n.674+28T>A
NR_169729.1:n.1302T>A
NR_169730.1:n.1205T>A
NR_169731.1:n.432-2347T>A
NR_169732.1:n.328+28T>A
NR_169733.1:n.386+28T>A
NR_169734.1:n.410+28T>A