Canonical Allele Identifier: CA322311022

Gene: PPIL2

Linked Data

• dbSNP Id: rs914168687
• MyVariant Identifiers: chr22:g.22012578G>C (hg19) ; chr22:g.21658289G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658289G>C , CM000684.2:g.21658289G>C	GRCh38
NC_000022.10:g.22012578G>C , CM000684.1:g.22012578G>C	GRCh37
NC_000022.9:g.20342578G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.186G>C
ENST00000498589.1:n.366G>C
XM_017029165.1:c.501G>C	XP_016884654.1:p.Gln167His
NR_169729.1:n.1101G>C
NR_169730.1:n.1004G>C
NR_169731.1:n.432-2548G>C
NR_169732.1:n.155G>C
NR_169733.1:n.214-1G>C
NR_169734.1:n.237G>C