Canonical Allele Identifier: CA2655514992
Gene: PPIL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658592G>T , CM000684.2:g.21658592G>T GRCh38
NC_000022.10:g.22012881G>T , CM000684.1:g.22012881G>T GRCh37
NC_000022.9:g.20342881G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+203G>T
ENST00000498589.1:n.540-51G>T
XM_017029165.1:c.674+130G>T XP_016884654.1:n.674+130G>T
NR_169729.1:n.1404G>T
NR_169730.1:n.1307G>T
NR_169731.1:n.432-2245G>T
NR_169732.1:n.328+130G>T
NR_169733.1:n.387-51G>T
NR_169734.1:n.411-51G>T