Canonical Allele Identifier: CA513535150
Gene: PPIL2 HGNC NCBI

Linked Data

gnomAD v4: 22-21658288-A-G
MyVariant Identifiers: chr22:g.22012577A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658288A>G , CM000684.2:g.21658288A>G GRCh38
NC_000022.10:g.22012577A>G , CM000684.1:g.22012577A>G GRCh37
NC_000022.9:g.20342577A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641967.1:n.185A>G
ENST00000498589.1:n.365A>G
XM_017029165.1:c.500A>G XP_016884654.1:p.Gln167Arg
NR_169729.1:n.1100A>G
NR_169730.1:n.1003A>G
NR_169731.1:n.432-2549A>G
NR_169732.1:n.154A>G
NR_169733.1:n.214-2A>G
NR_169734.1:n.236A>G
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