Canonical Allele Identifier: CA2396906880
Gene: PPIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658504A= , CM000684.2:g.21658504A= GRCh38
NC_000022.10:g.22012793A= , CM000684.1:g.22012793A= GRCh37
NC_000022.9:g.20342793A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641967.1:n.286+115A=
ENST00000498589.1:n.539+42A=
XM_017029165.1:c.674+42A= XP_016884654.1:n.674+42A=
NR_169729.1:n.1316A=
NR_169730.1:n.1219A=
NR_169731.1:n.432-2333A=
NR_169732.1:n.328+42A=
NR_169733.1:n.386+42A=
NR_169734.1:n.410+42A=