Canonical Allele Identifier: CA513535346
Gene: PPIL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.22012645C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658356C>A , CM000684.2:g.21658356C>A GRCh38
NC_000022.10:g.22012645C>A , CM000684.1:g.22012645C>A GRCh37
NC_000022.9:g.20342645C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.253C>A
ENST00000498589.1:n.433C>A
XM_017029165.1:c.568C>A XP_016884654.1:p.Gln190Lys
NR_169729.1:n.1168C>A
NR_169730.1:n.1071C>A
NR_169731.1:n.432-2481C>A
NR_169732.1:n.222C>A
NR_169733.1:n.280C>A
NR_169734.1:n.304C>A