Canonical Allele Identifier: CA513535102

Gene: PPIL2

Linked Data

• dbSNP Id: rs1601479488
• MyVariant Identifiers: chr22:g.22012561T>G (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.169T>G
ENST00000498589.1:n.349T>G
XM_017029165.1:c.484T>G	XP_016884654.1:p.Phe162Val
NR_169729.1:n.1084T>G
NR_169730.1:n.987T>G
NR_169731.1:n.432-2565T>G
NR_169732.1:n.138T>G
NR_169733.1:n.214-18T>G
NR_169734.1:n.220T>G