Canonical Allele Identifier: CA513535490
Gene: PPIL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.22012691C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658402C>T , CM000684.2:g.21658402C>T GRCh38
NC_000022.10:g.22012691C>T , CM000684.1:g.22012691C>T GRCh37
NC_000022.9:g.20342691C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+13C>T
ENST00000498589.1:n.479C>T
XM_017029165.1:c.614C>T XP_016884654.1:p.Pro205Leu
NR_169729.1:n.1214C>T
NR_169730.1:n.1117C>T
NR_169731.1:n.432-2435C>T
NR_169732.1:n.268C>T
NR_169733.1:n.326C>T
NR_169734.1:n.350C>T