Canonical Allele Identifier: CA2818468566
Gene: PPIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658487G>C , CM000684.2:g.21658487G>C GRCh38
NC_000022.10:g.22012776G>C , CM000684.1:g.22012776G>C GRCh37
NC_000022.9:g.20342776G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+98G>C
ENST00000498589.1:n.539+25G>C
XM_017029165.1:c.674+25G>C XP_016884654.1:n.674+25G>C
NR_169729.1:n.1299G>C
NR_169730.1:n.1202G>C
NR_169731.1:n.432-2350G>C
NR_169732.1:n.328+25G>C
NR_169733.1:n.386+25G>C
NR_169734.1:n.410+25G>C