Canonical Allele Identifier: CA513535482
Gene: PPIL2 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+10A>T
ENST00000498589.1:n.476A>T
XM_017029165.1:c.611A>T XP_016884654.1:p.Gln204Leu
NR_169729.1:n.1211A>T
NR_169730.1:n.1114A>T
NR_169731.1:n.432-2438A>T
NR_169732.1:n.265A>T
NR_169733.1:n.323A>T
NR_169734.1:n.347A>T