Canonical Allele Identifier: CA513535504
Gene: PPIL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.22012694T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658405T>A , CM000684.2:g.21658405T>A GRCh38
NC_000022.10:g.22012694T>A , CM000684.1:g.22012694T>A GRCh37
NC_000022.9:g.20342694T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+16T>A
ENST00000498589.1:n.482T>A
XM_017029165.1:c.617T>A XP_016884654.1:p.Leu206His
NR_169729.1:n.1217T>A
NR_169730.1:n.1120T>A
NR_169731.1:n.432-2432T>A
NR_169732.1:n.271T>A
NR_169733.1:n.329T>A
NR_169734.1:n.353T>A
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