Canonical Allele Identifier: CA513535104
Gene: PPIL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.22012561T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658272T>A , CM000684.2:g.21658272T>A GRCh38
NC_000022.10:g.22012561T>A , CM000684.1:g.22012561T>A GRCh37
NC_000022.9:g.20342561T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.169T>A
ENST00000498589.1:n.349T>A
XM_017029165.1:c.484T>A XP_016884654.1:p.Phe162Ile
NR_169729.1:n.1084T>A
NR_169730.1:n.987T>A
NR_169731.1:n.432-2565T>A
NR_169732.1:n.138T>A
NR_169733.1:n.214-18T>A
NR_169734.1:n.220T>A