Canonical Allele Identifier: CA513535338

Gene: PPIL2

Linked Data

• MyVariant Identifiers: chr22:g.22012643A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658354A>C , CM000684.2:g.21658354A>C	GRCh38
NC_000022.10:g.22012643A>C , CM000684.1:g.22012643A>C	GRCh37
NC_000022.9:g.20342643A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.251A>C
ENST00000498589.1:n.431A>C
XM_017029165.1:c.566A>C	XP_016884654.1:p.Lys189Thr
NR_169729.1:n.1166A>C
NR_169730.1:n.1069A>C
NR_169731.1:n.432-2483A>C
NR_169732.1:n.220A>C
NR_169733.1:n.278A>C
NR_169734.1:n.302A>C