Canonical Allele Identifier: CA513535541
Gene: PPIL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.22012704G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658415G>T , CM000684.2:g.21658415G>T GRCh38
NC_000022.10:g.22012704G>T , CM000684.1:g.22012704G>T GRCh37
NC_000022.9:g.20342704G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+26G>T
ENST00000498589.1:n.492G>T
XM_017029165.1:c.627G>T XP_016884654.1:p.Leu209=
NR_169729.1:n.1227G>T
NR_169730.1:n.1130G>T
NR_169731.1:n.432-2422G>T
NR_169732.1:n.281G>T
NR_169733.1:n.339G>T
NR_169734.1:n.363G>T
Search 100 bp 5'
Search 100 bp 3'