Canonical Allele Identifier: CA513535597
Gene: PPIL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.22012722T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658433T>A , CM000684.2:g.21658433T>A GRCh38
NC_000022.10:g.22012722T>A , CM000684.1:g.22012722T>A GRCh37
NC_000022.9:g.20342722T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+44T>A
ENST00000498589.1:n.510T>A
XM_017029165.1:c.645T>A XP_016884654.1:p.Ser215=
NR_169729.1:n.1245T>A
NR_169730.1:n.1148T>A
NR_169731.1:n.432-2404T>A
NR_169732.1:n.299T>A
NR_169733.1:n.357T>A
NR_169734.1:n.381T>A
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