Canonical Allele Identifier: CA513535478

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012687C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658398C>T , CM000684.2:g.21658398C>T	GRCh38
NC_000022.10:g.22012687C>T , CM000684.1:g.22012687C>T	GRCh37
NC_000022.9:g.20342687C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000641967.1:n.286+9C>T
ENST00000498589.1:n.475C>T
XM_017029165.1:c.610C>T	XP_016884654.1:p.Gln204Ter
NR_169729.1:n.1210C>T
NR_169730.1:n.1113C>T
NR_169731.1:n.432-2439C>T
NR_169732.1:n.264C>T
NR_169733.1:n.322C>T
NR_169734.1:n.346C>T