Canonical Allele Identifier: CA2655514791

Gene: PPIL2

Linked Data

• gnomAD v4: 22-21658465-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658465G>C , CM000684.2:g.21658465G>C	GRCh38
NC_000022.10:g.22012754G>C , CM000684.1:g.22012754G>C	GRCh37
NC_000022.9:g.20342754G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.286+76G>C
ENST00000498589.1:n.539+3G>C
XM_017029165.1:c.674+3G>C	XP_016884654.1:n.674+3G>C
NR_169729.1:n.1277G>C
NR_169730.1:n.1180G>C
NR_169731.1:n.432-2372G>C
NR_169732.1:n.328+3G>C
NR_169733.1:n.386+3G>C
NR_169734.1:n.410+3G>C