Canonical Allele Identifier: CA2396906797
Gene: PPIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658285T= , CM000684.2:g.21658285T= GRCh38
NC_000022.10:g.22012574T= , CM000684.1:g.22012574T= GRCh37
NC_000022.9:g.20342574T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.182T=
ENST00000498589.1:n.362T=
XM_017029165.1:c.497T= XP_016884654.1:p.Val166=
NR_169729.1:n.1097T=
NR_169730.1:n.1000T=
NR_169731.1:n.432-2552T=
NR_169732.1:n.151T=
NR_169733.1:n.214-5T=
NR_169734.1:n.233T=