Canonical Allele Identifier: CA513535451

Gene: PPIL2

Linked Data

• dbSNP Id: rs2066219699
• gnomAD v3: 22-21658390-G-A
• gnomAD v4: 22-21658390-G-A
• MyVariant Identifiers: chr22:g.22012679G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658390G>A , CM000684.2:g.21658390G>A	GRCh38
NC_000022.10:g.22012679G>A , CM000684.1:g.22012679G>A	GRCh37
NC_000022.9:g.20342679G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.286+1G>A
ENST00000498589.1:n.467G>A
XM_017029165.1:c.602G>A	XP_016884654.1:p.Gly201Asp
NR_169729.1:n.1202G>A
NR_169730.1:n.1105G>A
NR_169731.1:n.432-2447G>A
NR_169732.1:n.256G>A
NR_169733.1:n.314G>A
NR_169734.1:n.338G>A