Canonical Allele Identifier: CA513535159

Gene: PPIL2

Linked Data

• dbSNP Id: rs2066218621
• gnomAD v4: 22-21658291-C-T
• MyVariant Identifiers: chr22:g.22012580C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658291C>T , CM000684.2:g.21658291C>T	GRCh38
NC_000022.10:g.22012580C>T , CM000684.1:g.22012580C>T	GRCh37
NC_000022.9:g.20342580C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.188C>T
ENST00000498589.1:n.368C>T
XM_017029165.1:c.503C>T	XP_016884654.1:p.Ala168Val
NR_169729.1:n.1103C>T
NR_169730.1:n.1006C>T
NR_169731.1:n.432-2546C>T
NR_169732.1:n.157C>T
NR_169733.1:n.215C>T
NR_169734.1:n.239C>T