Canonical Allele Identifier: CA513535223

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012603A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658314A>T , CM000684.2:g.21658314A>T	GRCh38
NC_000022.10:g.22012603A>T , CM000684.1:g.22012603A>T	GRCh37
NC_000022.9:g.20342603A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.211A>T
ENST00000498589.1:n.391A>T
XM_017029165.1:c.526A>T	XP_016884654.1:p.Met176Leu
NR_169729.1:n.1126A>T
NR_169730.1:n.1029A>T
NR_169731.1:n.432-2523A>T
NR_169732.1:n.180A>T
NR_169733.1:n.238A>T
NR_169734.1:n.262A>T