Canonical Allele Identifier: CA2655514298
Gene: PPIL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658237C>T , CM000684.2:g.21658237C>T GRCh38
NC_000022.10:g.22012526C>T , CM000684.1:g.22012526C>T GRCh37
NC_000022.9:g.20342526C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.163-29C>T
ENST00000498589.1:n.343-29C>T
XM_017029165.1:c.478-29C>T XP_016884654.1:n.478-29C>T
NR_169729.1:n.1049C>T
NR_169730.1:n.952C>T
NR_169731.1:n.432-2600C>T
NR_169732.1:n.132-29C>T
NR_169733.1:n.214-53C>T
NR_169734.1:n.214-29C>T