Canonical Allele Identifier: CA513535100
Gene: PPIL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.22012560G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658271G>C , CM000684.2:g.21658271G>C GRCh38
NC_000022.10:g.22012560G>C , CM000684.1:g.22012560G>C GRCh37
NC_000022.9:g.20342560G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.168G>C
ENST00000498589.1:n.348G>C
XM_017029165.1:c.483G>C XP_016884654.1:p.Lys161Asn
NR_169729.1:n.1083G>C
NR_169730.1:n.986G>C
NR_169731.1:n.432-2566G>C
NR_169732.1:n.137G>C
NR_169733.1:n.214-19G>C
NR_169734.1:n.219G>C