Canonical Allele Identifier: CA2396906800
Gene: PPIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658291C= , CM000684.2:g.21658291C= GRCh38
NC_000022.10:g.22012580C= , CM000684.1:g.22012580C= GRCh37
NC_000022.9:g.20342580C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.188C=
ENST00000498589.1:n.368C=
XM_017029165.1:c.503C= XP_016884654.1:p.Ala168=
NR_169729.1:n.1103C=
NR_169730.1:n.1006C=
NR_169731.1:n.432-2546C=
NR_169732.1:n.157C=
NR_169733.1:n.215C=
NR_169734.1:n.239C=