Canonical Allele Identifier: CA513535431

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012673C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658384C>T , CM000684.2:g.21658384C>T	GRCh38
NC_000022.10:g.22012673C>T , CM000684.1:g.22012673C>T	GRCh37
NC_000022.9:g.20342673C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.281C>T
ENST00000498589.1:n.461C>T
XM_017029165.1:c.596C>T	XP_016884654.1:p.Ser199Phe
NR_169729.1:n.1196C>T
NR_169730.1:n.1099C>T
NR_169731.1:n.432-2453C>T
NR_169732.1:n.250C>T
NR_169733.1:n.308C>T
NR_169734.1:n.332C>T