Canonical Allele Identifier: CA2396906858
Gene: PPIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658428G= , CM000684.2:g.21658428G= GRCh38
NC_000022.10:g.22012717G= , CM000684.1:g.22012717G= GRCh37
NC_000022.9:g.20342717G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+39G=
ENST00000498589.1:n.505G=
XM_017029165.1:c.640G= XP_016884654.1:p.Gly214=
NR_169729.1:n.1240G=
NR_169730.1:n.1143G=
NR_169731.1:n.432-2409G=
NR_169732.1:n.294G=
NR_169733.1:n.352G=
NR_169734.1:n.376G=