Canonical Allele Identifier: CA513535486
Gene: PPIL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.22012689A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658400A>T , CM000684.2:g.21658400A>T GRCh38
NC_000022.10:g.22012689A>T , CM000684.1:g.22012689A>T GRCh37
NC_000022.9:g.20342689A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+11A>T
ENST00000498589.1:n.477A>T
XM_017029165.1:c.612A>T XP_016884654.1:p.Gln204His
NR_169729.1:n.1212A>T
NR_169730.1:n.1115A>T
NR_169731.1:n.432-2437A>T
NR_169732.1:n.266A>T
NR_169733.1:n.324A>T
NR_169734.1:n.348A>T