Canonical Allele Identifier: CA513535602

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012723G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658434G>C , CM000684.2:g.21658434G>C	GRCh38
NC_000022.10:g.22012723G>C , CM000684.1:g.22012723G>C	GRCh37
NC_000022.9:g.20342723G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.286+45G>C
ENST00000498589.1:n.511G>C
XM_017029165.1:c.646G>C	XP_016884654.1:p.Glu216Gln
NR_169729.1:n.1246G>C
NR_169730.1:n.1149G>C
NR_169731.1:n.432-2403G>C
NR_169732.1:n.300G>C
NR_169733.1:n.358G>C
NR_169734.1:n.382G>C