Canonical Allele Identifier: CA2396906752
Gene: PPIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658208G= , CM000684.2:g.21658208G= GRCh38
NC_000022.10:g.22012497G= , CM000684.1:g.22012497G= GRCh37
NC_000022.9:g.20342497G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.163-58G=
ENST00000498589.1:n.343-58G=
XM_017029165.1:c.478-58G= XP_016884654.1:n.478-58G=
NR_169729.1:n.1020G=
NR_169730.1:n.923G=
NR_169731.1:n.432-2629G=
NR_169732.1:n.132-58G=
NR_169733.1:n.214-82G=
NR_169734.1:n.214-58G=