Canonical Allele Identifier: CA513535488

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012690C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658401C>A , CM000684.2:g.21658401C>A	GRCh38
NC_000022.10:g.22012690C>A , CM000684.1:g.22012690C>A	GRCh37
NC_000022.9:g.20342690C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000641967.1:n.286+12C>A
ENST00000498589.1:n.478C>A
XM_017029165.1:c.613C>A	XP_016884654.1:p.Pro205Thr
NR_169729.1:n.1213C>A
NR_169730.1:n.1116C>A
NR_169731.1:n.432-2436C>A
NR_169732.1:n.267C>A
NR_169733.1:n.325C>A
NR_169734.1:n.349C>A