Canonical Allele Identifier: CA513535437
Gene: PPIL2 HGNC NCBI

Linked Data

gnomAD v4: 22-21658386-C-A
MyVariant Identifiers: chr22:g.22012675C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658386C>A , CM000684.2:g.21658386C>A GRCh38
NC_000022.10:g.22012675C>A , CM000684.1:g.22012675C>A GRCh37
NC_000022.9:g.20342675C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.283C>A
ENST00000498589.1:n.463C>A
XM_017029165.1:c.598C>A XP_016884654.1:p.Arg200=
NR_169729.1:n.1198C>A
NR_169730.1:n.1101C>A
NR_169731.1:n.432-2451C>A
NR_169732.1:n.252C>A
NR_169733.1:n.310C>A
NR_169734.1:n.334C>A
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