Canonical Allele Identifier: CA2396906892
Gene: PPIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658530G= , CM000684.2:g.21658530G= GRCh38
NC_000022.10:g.22012819G= , CM000684.1:g.22012819G= GRCh37
NC_000022.9:g.20342819G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+141G=
ENST00000498589.1:n.539+68G=
XM_017029165.1:c.674+68G= XP_016884654.1:n.674+68G=
NR_169729.1:n.1342G=
NR_169730.1:n.1245G=
NR_169731.1:n.432-2307G=
NR_169732.1:n.328+68G=
NR_169733.1:n.386+68G=
NR_169734.1:n.410+68G=