Canonical Allele Identifier: CA2396906785
Gene: PPIL2 HGNC NCBI

Linked Data

dbSNP Id: rs2066218261
gnomAD v4: 22-21658262-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658262G>T , CM000684.2:g.21658262G>T GRCh38
NC_000022.10:g.22012551G>T , CM000684.1:g.22012551G>T GRCh37
NC_000022.9:g.20342551G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.163-4G>T
ENST00000498589.1:n.343-4G>T
XM_017029165.1:c.478-4G>T XP_016884654.1:n.478-4G>T
NR_169729.1:n.1074G>T
NR_169730.1:n.977G>T
NR_169731.1:n.432-2575G>T
NR_169732.1:n.132-4G>T
NR_169733.1:n.214-28G>T
NR_169734.1:n.214-4G>T
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