Canonical Allele Identifier: CA2396906885
Gene: PPIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658509G= , CM000684.2:g.21658509G= GRCh38
NC_000022.10:g.22012798G= , CM000684.1:g.22012798G= GRCh37
NC_000022.9:g.20342798G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641967.1:n.286+120G=
ENST00000498589.1:n.539+47G=
XM_017029165.1:c.674+47G= XP_016884654.1:n.674+47G=
NR_169729.1:n.1321G=
NR_169730.1:n.1224G=
NR_169731.1:n.432-2328G=
NR_169732.1:n.328+47G=
NR_169733.1:n.386+47G=
NR_169734.1:n.410+47G=