Canonical Allele Identifier: CA513535138

Gene: PPIL2

Linked Data

• gnomAD v4: 22-21658284-G-A
• MyVariant Identifiers: chr22:g.22012573G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658284G>A , CM000684.2:g.21658284G>A	GRCh38
NC_000022.10:g.22012573G>A , CM000684.1:g.22012573G>A	GRCh37
NC_000022.9:g.20342573G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000641967.1:n.181G>A
ENST00000498589.1:n.361G>A
XM_017029165.1:c.496G>A	XP_016884654.1:p.Val166Met
NR_169729.1:n.1096G>A
NR_169730.1:n.999G>A
NR_169731.1:n.432-2553G>A
NR_169732.1:n.150G>A
NR_169733.1:n.214-6G>A
NR_169734.1:n.232G>A