Canonical Allele Identifier: CA513535483
Gene: PPIL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.22012688A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658399A>G , CM000684.2:g.21658399A>G GRCh38
NC_000022.10:g.22012688A>G , CM000684.1:g.22012688A>G GRCh37
NC_000022.9:g.20342688A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+10A>G
ENST00000498589.1:n.476A>G
XM_017029165.1:c.611A>G XP_016884654.1:p.Gln204Arg
NR_169729.1:n.1211A>G
NR_169730.1:n.1114A>G
NR_169731.1:n.432-2438A>G
NR_169732.1:n.265A>G
NR_169733.1:n.323A>G
NR_169734.1:n.347A>G