Canonical Allele Identifier: CA513535625

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012731T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658442T>G , CM000684.2:g.21658442T>G	GRCh38
NC_000022.10:g.22012731T>G , CM000684.1:g.22012731T>G	GRCh37
NC_000022.9:g.20342731T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.286+53T>G
ENST00000498589.1:n.519T>G
XM_017029165.1:c.654T>G	XP_016884654.1:p.Ser218Arg
NR_169729.1:n.1254T>G
NR_169730.1:n.1157T>G
NR_169731.1:n.432-2395T>G
NR_169732.1:n.308T>G
NR_169733.1:n.366T>G
NR_169734.1:n.390T>G