Canonical Allele Identifier: CA513535187

Gene: PPIL2

Linked Data

• gnomAD v4: 22-21658302-C-A
• MyVariant Identifiers: chr22:g.22012591C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658302C>A , CM000684.2:g.21658302C>A	GRCh38
NC_000022.10:g.22012591C>A , CM000684.1:g.22012591C>A	GRCh37
NC_000022.9:g.20342591C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.199C>A
ENST00000498589.1:n.379C>A
XM_017029165.1:c.514C>A	XP_016884654.1:p.His172Asn
NR_169729.1:n.1114C>A
NR_169730.1:n.1017C>A
NR_169731.1:n.432-2535C>A
NR_169732.1:n.168C>A
NR_169733.1:n.226C>A
NR_169734.1:n.250C>A