Canonical Allele Identifier: CA2396906877
Gene: PPIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658494C= , CM000684.2:g.21658494C= GRCh38
NC_000022.10:g.22012783C= , CM000684.1:g.22012783C= GRCh37
NC_000022.9:g.20342783C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641967.1:n.286+105C=
ENST00000498589.1:n.539+32C=
XM_017029165.1:c.674+32C= XP_016884654.1:n.674+32C=
NR_169729.1:n.1306C=
NR_169730.1:n.1209C=
NR_169731.1:n.432-2343C=
NR_169732.1:n.328+32C=
NR_169733.1:n.386+32C=
NR_169734.1:n.410+32C=