Canonical Allele Identifier: CA513535503

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012694T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658405T>C , CM000684.2:g.21658405T>C	GRCh38
NC_000022.10:g.22012694T>C , CM000684.1:g.22012694T>C	GRCh37
NC_000022.9:g.20342694T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000641967.1:n.286+16T>C
ENST00000498589.1:n.482T>C
XM_017029165.1:c.617T>C	XP_016884654.1:p.Leu206Pro
NR_169729.1:n.1217T>C
NR_169730.1:n.1120T>C
NR_169731.1:n.432-2432T>C
NR_169732.1:n.271T>C
NR_169733.1:n.329T>C
NR_169734.1:n.353T>C