Canonical Allele Identifier: CA513535156

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012579G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658290G>C , CM000684.2:g.21658290G>C	GRCh38
NC_000022.10:g.22012579G>C , CM000684.1:g.22012579G>C	GRCh37
NC_000022.9:g.20342579G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000641967.1:n.187G>C
ENST00000498589.1:n.367G>C
XM_017029165.1:c.502G>C	XP_016884654.1:p.Ala168Pro
NR_169729.1:n.1102G>C
NR_169730.1:n.1005G>C
NR_169731.1:n.432-2547G>C
NR_169732.1:n.156G>C
NR_169733.1:n.214G>C
NR_169734.1:n.238G>C