Canonical Allele Identifier: CA513535447

Gene: PPIL2

Linked Data

• gnomAD v4: 22-21658389-G-T
• MyVariant Identifiers: chr22:g.22012678G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658389G>T , CM000684.2:g.21658389G>T	GRCh38
NC_000022.10:g.22012678G>T , CM000684.1:g.22012678G>T	GRCh37
NC_000022.9:g.20342678G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.286G>T
ENST00000498589.1:n.466G>T
XM_017029165.1:c.601G>T	XP_016884654.1:p.Gly201Cys
NR_169729.1:n.1201G>T
NR_169730.1:n.1104G>T
NR_169731.1:n.432-2448G>T
NR_169732.1:n.255G>T
NR_169733.1:n.313G>T
NR_169734.1:n.337G>T