Canonical Allele Identifier: CA513535348

Gene: PPIL2

Linked Data

• dbSNP Id: rs2066219246
• gnomAD v3: 22-21658357-A-G
• gnomAD v4: 22-21658357-A-G
• MyVariant Identifiers: chr22:g.22012646A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658357A>G , CM000684.2:g.21658357A>G	GRCh38
NC_000022.10:g.22012646A>G , CM000684.1:g.22012646A>G	GRCh37
NC_000022.9:g.20342646A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.254A>G
ENST00000498589.1:n.434A>G
XM_017029165.1:c.569A>G	XP_016884654.1:p.Gln190Arg
NR_169729.1:n.1169A>G
NR_169730.1:n.1072A>G
NR_169731.1:n.432-2480A>G
NR_169732.1:n.223A>G
NR_169733.1:n.281A>G
NR_169734.1:n.305A>G