Canonical Allele Identifier: CA513535089

Gene: PPIL2

Linked Data

• gnomAD v4: 22-21658267-C-A
• MyVariant Identifiers: chr22:g.22012556C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658267C>A , CM000684.2:g.21658267C>A	GRCh38
NC_000022.10:g.22012556C>A , CM000684.1:g.22012556C>A	GRCh37
NC_000022.9:g.20342556C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.164C>A
ENST00000498589.1:n.344C>A
XM_017029165.1:c.479C>A	XP_016884654.1:p.Ala160Glu
NR_169729.1:n.1079C>A
NR_169730.1:n.982C>A
NR_169731.1:n.432-2570C>A
NR_169732.1:n.133C>A
NR_169733.1:n.214-23C>A
NR_169734.1:n.215C>A