Canonical Allele Identifier: CA513535087

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012556C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658267C>T , CM000684.2:g.21658267C>T	GRCh38
NC_000022.10:g.22012556C>T , CM000684.1:g.22012556C>T	GRCh37
NC_000022.9:g.20342556C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.164C>T
ENST00000498589.1:n.344C>T
XM_017029165.1:c.479C>T	XP_016884654.1:p.Ala160Val
NR_169729.1:n.1079C>T
NR_169730.1:n.982C>T
NR_169731.1:n.432-2570C>T
NR_169732.1:n.133C>T
NR_169733.1:n.214-23C>T
NR_169734.1:n.215C>T