Canonical Allele Identifier: CA513535593
Gene: PPIL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.22012721C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658432C>A , CM000684.2:g.21658432C>A GRCh38
NC_000022.10:g.22012721C>A , CM000684.1:g.22012721C>A GRCh37
NC_000022.9:g.20342721C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+43C>A
ENST00000498589.1:n.509C>A
XM_017029165.1:c.644C>A XP_016884654.1:p.Ser215Tyr
NR_169729.1:n.1244C>A
NR_169730.1:n.1147C>A
NR_169731.1:n.432-2405C>A
NR_169732.1:n.298C>A
NR_169733.1:n.356C>A
NR_169734.1:n.380C>A