Canonical Allele Identifier: CA513535487

Gene: PPIL2

Linked Data

• gnomAD v4: 22-21658401-C-T
• MyVariant Identifiers: chr22:g.22012690C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658401C>T , CM000684.2:g.21658401C>T	GRCh38
NC_000022.10:g.22012690C>T , CM000684.1:g.22012690C>T	GRCh37
NC_000022.9:g.20342690C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000641967.1:n.286+12C>T
ENST00000498589.1:n.478C>T
XM_017029165.1:c.613C>T	XP_016884654.1:p.Pro205Ser
NR_169729.1:n.1213C>T
NR_169730.1:n.1116C>T
NR_169731.1:n.432-2436C>T
NR_169732.1:n.267C>T
NR_169733.1:n.325C>T
NR_169734.1:n.349C>T