Canonical Allele Identifier: CA513535439

Gene: PPIL2

Linked Data

• dbSNP Id: rs2148480254
• gnomAD v4: 22-21658386-C-T
• MyVariant Identifiers: chr22:g.22012675C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658386C>T , CM000684.2:g.21658386C>T	GRCh38
NC_000022.10:g.22012675C>T , CM000684.1:g.22012675C>T	GRCh37
NC_000022.9:g.20342675C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.283C>T
ENST00000498589.1:n.463C>T
XM_017029165.1:c.598C>T	XP_016884654.1:p.Arg200Trp
NR_169729.1:n.1198C>T
NR_169730.1:n.1101C>T
NR_169731.1:n.432-2451C>T
NR_169732.1:n.252C>T
NR_169733.1:n.310C>T
NR_169734.1:n.334C>T