Canonical Allele Identifier: CA513535116

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012565T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658276T>A , CM000684.2:g.21658276T>A	GRCh38
NC_000022.10:g.22012565T>A , CM000684.1:g.22012565T>A	GRCh37
NC_000022.9:g.20342565T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.173T>A
ENST00000498589.1:n.353T>A
XM_017029165.1:c.488T>A	XP_016884654.1:p.Phe163Tyr
NR_169729.1:n.1088T>A
NR_169730.1:n.991T>A
NR_169731.1:n.432-2561T>A
NR_169732.1:n.142T>A
NR_169733.1:n.214-14T>A
NR_169734.1:n.224T>A