Canonical Allele Identifier: CA513535620

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012729A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658440A>C , CM000684.2:g.21658440A>C	GRCh38
NC_000022.10:g.22012729A>C , CM000684.1:g.22012729A>C	GRCh37
NC_000022.9:g.20342729A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.286+51A>C
ENST00000498589.1:n.517A>C
XM_017029165.1:c.652A>C	XP_016884654.1:p.Ser218Arg
NR_169729.1:n.1252A>C
NR_169730.1:n.1155A>C
NR_169731.1:n.432-2397A>C
NR_169732.1:n.306A>C
NR_169733.1:n.364A>C
NR_169734.1:n.388A>C