Canonical Allele Identifier: CA2396906921
Gene: PPIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658593A= , CM000684.2:g.21658593A= GRCh38
NC_000022.10:g.22012882A= , CM000684.1:g.22012882A= GRCh37
NC_000022.9:g.20342882A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+204A=
ENST00000498589.1:n.540-50A=
XM_017029165.1:c.674+131A= XP_016884654.1:n.674+131A=
NR_169729.1:n.1405A=
NR_169730.1:n.1308A=
NR_169731.1:n.432-2244A=
NR_169732.1:n.328+131A=
NR_169733.1:n.387-50A=
NR_169734.1:n.411-50A=