Canonical Allele Identifier: CA513535649

Gene: PPIL2

Linked Data

• gnomAD v4: 22-21658449-A-G
• MyVariant Identifiers: chr22:g.22012738A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658449A>G , CM000684.2:g.21658449A>G	GRCh38
NC_000022.10:g.22012738A>G , CM000684.1:g.22012738A>G	GRCh37
NC_000022.9:g.20342738A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.286+60A>G
ENST00000498589.1:n.526A>G
XM_017029165.1:c.661A>G	XP_016884654.1:p.Arg221Gly
NR_169729.1:n.1261A>G
NR_169730.1:n.1164A>G
NR_169731.1:n.432-2388A>G
NR_169732.1:n.315A>G
NR_169733.1:n.373A>G
NR_169734.1:n.397A>G