Canonical Allele Identifier: CA513535465
Gene: PPIL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.22012682A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658393A>T , CM000684.2:g.21658393A>T GRCh38
NC_000022.10:g.22012682A>T , CM000684.1:g.22012682A>T GRCh37
NC_000022.9:g.20342682A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+4A>T
ENST00000498589.1:n.470A>T
XM_017029165.1:c.605A>T XP_016884654.1:p.Glu202Val
NR_169729.1:n.1205A>T
NR_169730.1:n.1108A>T
NR_169731.1:n.432-2444A>T
NR_169732.1:n.259A>T
NR_169733.1:n.317A>T
NR_169734.1:n.341A>T