Canonical Allele Identifier: CA513535111

Gene: PPIL2

Linked Data

• dbSNP Id: rs2066218438
• gnomAD v4: 22-21658275-T-C
• MyVariant Identifiers: chr22:g.22012564T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658275T>C , CM000684.2:g.21658275T>C	GRCh38
NC_000022.10:g.22012564T>C , CM000684.1:g.22012564T>C	GRCh37
NC_000022.9:g.20342564T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.172T>C
ENST00000498589.1:n.352T>C
XM_017029165.1:c.487T>C	XP_016884654.1:p.Phe163Leu
NR_169729.1:n.1087T>C
NR_169730.1:n.990T>C
NR_169731.1:n.432-2562T>C
NR_169732.1:n.141T>C
NR_169733.1:n.214-15T>C
NR_169734.1:n.223T>C