Canonical Allele Identifier: CA2818468574
Gene: PPIL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658552G>T , CM000684.2:g.21658552G>T GRCh38
NC_000022.10:g.22012841G>T , CM000684.1:g.22012841G>T GRCh37
NC_000022.9:g.20342841G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+163G>T
ENST00000498589.1:n.540-91G>T
XM_017029165.1:c.674+90G>T XP_016884654.1:n.674+90G>T
NR_169729.1:n.1364G>T
NR_169730.1:n.1267G>T
NR_169731.1:n.432-2285G>T
NR_169732.1:n.328+90G>T
NR_169733.1:n.387-91G>T
NR_169734.1:n.411-91G>T