Canonical Allele Identifier: CA2396906845
Gene: PPIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658395G= , CM000684.2:g.21658395G= GRCh38
NC_000022.10:g.22012684G= , CM000684.1:g.22012684G= GRCh37
NC_000022.9:g.20342684G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641967.1:n.286+6G=
ENST00000498589.1:n.472G=
XM_017029165.1:c.607G= XP_016884654.1:p.Asp203=
NR_169729.1:n.1207G=
NR_169730.1:n.1110G=
NR_169731.1:n.432-2442G=
NR_169732.1:n.261G=
NR_169733.1:n.319G=
NR_169734.1:n.343G=