Canonical Allele Identifier: CA513535169
Gene: PPIL2 HGNC NCBI

Linked Data

dbSNP Id: rs1174184507
MyVariant Identifiers: chr22:g.22012584G>A (hg19) chr22:g.21658295G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658295G>A , CM000684.2:g.21658295G>A GRCh38
NC_000022.10:g.22012584G>A , CM000684.1:g.22012584G>A GRCh37
NC_000022.9:g.20342584G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.192G>A
ENST00000498589.1:n.372G>A
XM_017029165.1:c.507G>A XP_016884654.1:p.Glu169=
NR_169729.1:n.1107G>A
NR_169730.1:n.1010G>A
NR_169731.1:n.432-2542G>A
NR_169732.1:n.161G>A
NR_169733.1:n.219G>A
NR_169734.1:n.243G>A
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