Canonical Allele Identifier: CA1024327002

Gene: PPIL2

Linked Data

• dbSNP Id: rs2066220693
• gnomAD v3: 22-21658494-C-T
• gnomAD v4: 22-21658494-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658494C>T , CM000684.2:g.21658494C>T	GRCh38
NC_000022.10:g.22012783C>T , CM000684.1:g.22012783C>T	GRCh37
NC_000022.9:g.20342783C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000641967.1:n.286+105C>T
ENST00000498589.1:n.539+32C>T
XM_017029165.1:c.674+32C>T	XP_016884654.1:n.674+32C>T
NR_169729.1:n.1306C>T
NR_169730.1:n.1209C>T
NR_169731.1:n.432-2343C>T
NR_169732.1:n.328+32C>T
NR_169733.1:n.386+32C>T
NR_169734.1:n.410+32C>T