Canonical Allele Identifier: CA751583066

Gene: PPIL2

Linked Data

• dbSNP Id: rs1463982831
• gnomAD v3: 22-21658491-T-G
• gnomAD v4: 22-21658491-T-G
• MyVariant Identifiers: chr22:g.22012780T>G (hg19) ; chr22:g.21658491T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658491T>G , CM000684.2:g.21658491T>G	GRCh38
NC_000022.10:g.22012780T>G , CM000684.1:g.22012780T>G	GRCh37
NC_000022.9:g.20342780T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000641967.1:n.286+102T>G
ENST00000498589.1:n.539+29T>G
XM_017029165.1:c.674+29T>G	XP_016884654.1:n.674+29T>G
NR_169729.1:n.1303T>G
NR_169730.1:n.1206T>G
NR_169731.1:n.432-2346T>G
NR_169732.1:n.328+29T>G
NR_169733.1:n.386+29T>G
NR_169734.1:n.410+29T>G