Canonical Allele Identifier: CA2396906881
Gene: PPIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658507A= , CM000684.2:g.21658507A= GRCh38
NC_000022.10:g.22012796A= , CM000684.1:g.22012796A= GRCh37
NC_000022.9:g.20342796A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641967.1:n.286+118A=
ENST00000498589.1:n.539+45A=
XM_017029165.1:c.674+45A= XP_016884654.1:n.674+45A=
NR_169729.1:n.1319A=
NR_169730.1:n.1222A=
NR_169731.1:n.432-2330A=
NR_169732.1:n.328+45A=
NR_169733.1:n.386+45A=
NR_169734.1:n.410+45A=