Canonical Allele Identifier: CA2396906849
Gene: PPIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658409C= , CM000684.2:g.21658409C= GRCh38
NC_000022.10:g.22012698C= , CM000684.1:g.22012698C= GRCh37
NC_000022.9:g.20342698C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+20C=
ENST00000498589.1:n.486C=
XM_017029165.1:c.621C= XP_016884654.1:p.Pro207=
NR_169729.1:n.1221C=
NR_169730.1:n.1124C=
NR_169731.1:n.432-2428C=
NR_169732.1:n.275C=
NR_169733.1:n.333C=
NR_169734.1:n.357C=