Canonical Allele Identifier: CA513535475

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012686T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658397T>A , CM000684.2:g.21658397T>A	GRCh38
NC_000022.10:g.22012686T>A , CM000684.1:g.22012686T>A	GRCh37
NC_000022.9:g.20342686T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.286+8T>A
ENST00000498589.1:n.474T>A
XM_017029165.1:c.609T>A	XP_016884654.1:p.Asp203Glu
NR_169729.1:n.1209T>A
NR_169730.1:n.1112T>A
NR_169731.1:n.432-2440T>A
NR_169732.1:n.263T>A
NR_169733.1:n.321T>A
NR_169734.1:n.345T>A