Canonical Allele Identifier: CA2655514855

Gene: PPIL2

Linked Data

• gnomAD v4: 22-21658499-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658499C>A , CM000684.2:g.21658499C>A	GRCh38
NC_000022.10:g.22012788C>A , CM000684.1:g.22012788C>A	GRCh37
NC_000022.9:g.20342788C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000641967.1:n.286+110C>A
ENST00000498589.1:n.539+37C>A
XM_017029165.1:c.674+37C>A	XP_016884654.1:n.674+37C>A
NR_169729.1:n.1311C>A
NR_169730.1:n.1214C>A
NR_169731.1:n.432-2338C>A
NR_169732.1:n.328+37C>A
NR_169733.1:n.386+37C>A
NR_169734.1:n.410+37C>A