Canonical Allele Identifier: CA513535142

Gene: PPIL2

Linked Data

• dbSNP Id: rs2066218539
• gnomAD v4: 22-21658285-T-C
• MyVariant Identifiers: chr22:g.22012574T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.21658285T>C , CM000684.2:g.21658285T>C	GRCh38
NC_000022.10:g.22012574T>C , CM000684.1:g.22012574T>C	GRCh37
NC_000022.9:g.20342574T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641967.1:n.182T>C
ENST00000498589.1:n.362T>C
XM_017029165.1:c.497T>C	XP_016884654.1:p.Val166Ala
NR_169729.1:n.1097T>C
NR_169730.1:n.1000T>C
NR_169731.1:n.432-2552T>C
NR_169732.1:n.151T>C
NR_169733.1:n.214-5T>C
NR_169734.1:n.233T>C