Canonical Allele Identifier: CA513535385

Gene: PPIL2

Linked Data

• gnomAD v4: 22-21658369-G-T
• MyVariant Identifiers: chr22:g.22012658G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658369G>T , CM000684.2:g.21658369G>T	GRCh38
NC_000022.10:g.22012658G>T , CM000684.1:g.22012658G>T	GRCh37
NC_000022.9:g.20342658G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.266G>T
ENST00000498589.1:n.446G>T
XM_017029165.1:c.581G>T	XP_016884654.1:p.Arg194Leu
NR_169729.1:n.1181G>T
NR_169730.1:n.1084G>T
NR_169731.1:n.432-2468G>T
NR_169732.1:n.235G>T
NR_169733.1:n.293G>T
NR_169734.1:n.317G>T