Canonical Allele Identifier: CA2655514866
Gene: PPIL2 HGNC NCBI

Linked Data

gnomAD v4: 22-21658506-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658506C>A , CM000684.2:g.21658506C>A GRCh38
NC_000022.10:g.22012795C>A , CM000684.1:g.22012795C>A GRCh37
NC_000022.9:g.20342795C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641967.1:n.286+117C>A
ENST00000498589.1:n.539+44C>A
XM_017029165.1:c.674+44C>A XP_016884654.1:n.674+44C>A
NR_169729.1:n.1318C>A
NR_169730.1:n.1221C>A
NR_169731.1:n.432-2331C>A
NR_169732.1:n.328+44C>A
NR_169733.1:n.386+44C>A
NR_169734.1:n.410+44C>A
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