Canonical Allele Identifier: CA513535106

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012562T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658273T>A , CM000684.2:g.21658273T>A	GRCh38
NC_000022.10:g.22012562T>A , CM000684.1:g.22012562T>A	GRCh37
NC_000022.9:g.20342562T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.170T>A
ENST00000498589.1:n.350T>A
XM_017029165.1:c.485T>A	XP_016884654.1:p.Phe162Tyr
NR_169729.1:n.1085T>A
NR_169730.1:n.988T>A
NR_169731.1:n.432-2564T>A
NR_169732.1:n.139T>A
NR_169733.1:n.214-17T>A
NR_169734.1:n.221T>A