Canonical Allele Identifier: CA2396906775
Gene: PPIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658237C= , CM000684.2:g.21658237C= GRCh38
NC_000022.10:g.22012526C= , CM000684.1:g.22012526C= GRCh37
NC_000022.9:g.20342526C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.163-29C=
ENST00000498589.1:n.343-29C=
XM_017029165.1:c.478-29C= XP_016884654.1:n.478-29C=
NR_169729.1:n.1049C=
NR_169730.1:n.952C=
NR_169731.1:n.432-2600C=
NR_169732.1:n.132-29C=
NR_169733.1:n.214-53C=
NR_169734.1:n.214-29C=