Canonical Allele Identifier: CA2655514967
Gene: PPIL2 HGNC NCBI

Linked Data

gnomAD v4: 22-21658561-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658561C>A , CM000684.2:g.21658561C>A GRCh38
NC_000022.10:g.22012850C>A , CM000684.1:g.22012850C>A GRCh37
NC_000022.9:g.20342850C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+172C>A
ENST00000498589.1:n.540-82C>A
XM_017029165.1:c.674+99C>A XP_016884654.1:n.674+99C>A
NR_169729.1:n.1373C>A
NR_169730.1:n.1276C>A
NR_169731.1:n.432-2276C>A
NR_169732.1:n.328+99C>A
NR_169733.1:n.387-82C>A
NR_169734.1:n.411-82C>A
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