Canonical Allele Identifier: CA322311085
Gene: PPIL2 HGNC NCBI

Linked Data

dbSNP Id: rs1015521313
gnomAD v3: 22-21658385-C-T
gnomAD v4: 22-21658385-C-T
MyVariant Identifiers: chr22:g.22012674C>T (hg19) chr22:g.21658385C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658385C>T , CM000684.2:g.21658385C>T GRCh38
NC_000022.10:g.22012674C>T , CM000684.1:g.22012674C>T GRCh37
NC_000022.9:g.20342674C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.282C>T
ENST00000498589.1:n.462C>T
XM_017029165.1:c.597C>T XP_016884654.1:p.Ser199=
NR_169729.1:n.1197C>T
NR_169730.1:n.1100C>T
NR_169731.1:n.432-2452C>T
NR_169732.1:n.251C>T
NR_169733.1:n.309C>T
NR_169734.1:n.333C>T
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