Canonical Allele Identifier: CA513535175
Gene: PPIL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.22012586T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658297T>A , CM000684.2:g.21658297T>A GRCh38
NC_000022.10:g.22012586T>A , CM000684.1:g.22012586T>A GRCh37
NC_000022.9:g.20342586T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.194T>A
ENST00000498589.1:n.374T>A
XM_017029165.1:c.509T>A XP_016884654.1:p.Leu170Gln
NR_169729.1:n.1109T>A
NR_169730.1:n.1012T>A
NR_169731.1:n.432-2540T>A
NR_169732.1:n.163T>A
NR_169733.1:n.221T>A
NR_169734.1:n.245T>A