Canonical Allele Identifier: CA2396906846
Gene: PPIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658400A= , CM000684.2:g.21658400A= GRCh38
NC_000022.10:g.22012689A= , CM000684.1:g.22012689A= GRCh37
NC_000022.9:g.20342689A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+11A=
ENST00000498589.1:n.477A=
XM_017029165.1:c.612A= XP_016884654.1:p.Gln204=
NR_169729.1:n.1212A=
NR_169730.1:n.1115A=
NR_169731.1:n.432-2437A=
NR_169732.1:n.266A=
NR_169733.1:n.324A=
NR_169734.1:n.348A=