Canonical Allele Identifier: CA2655514849
Gene: PPIL2 HGNC NCBI

Linked Data

gnomAD v4: 22-21658495-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658495C>A , CM000684.2:g.21658495C>A GRCh38
NC_000022.10:g.22012784C>A , CM000684.1:g.22012784C>A GRCh37
NC_000022.9:g.20342784C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641967.1:n.286+106C>A
ENST00000498589.1:n.539+33C>A
XM_017029165.1:c.674+33C>A XP_016884654.1:n.674+33C>A
NR_169729.1:n.1307C>A
NR_169730.1:n.1210C>A
NR_169731.1:n.432-2342C>A
NR_169732.1:n.328+33C>A
NR_169733.1:n.386+33C>A
NR_169734.1:n.410+33C>A
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