Canonical Allele Identifier: CA2396906801
Gene: PPIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658293G= , CM000684.2:g.21658293G= GRCh38
NC_000022.10:g.22012582G= , CM000684.1:g.22012582G= GRCh37
NC_000022.9:g.20342582G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.190G=
ENST00000498589.1:n.370G=
XM_017029165.1:c.505G= XP_016884654.1:p.Glu169=
NR_169729.1:n.1105G=
NR_169730.1:n.1008G=
NR_169731.1:n.432-2544G=
NR_169732.1:n.159G=
NR_169733.1:n.217G=
NR_169734.1:n.241G=