Canonical Allele Identifier: CA513535444
Gene: PPIL2 HGNC NCBI

Linked Data

dbSNP Id: rs2066219670
MyVariant Identifiers: chr22:g.22012677G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658388G>A , CM000684.2:g.21658388G>A GRCh38
NC_000022.10:g.22012677G>A , CM000684.1:g.22012677G>A GRCh37
NC_000022.9:g.20342677G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.285G>A
ENST00000498589.1:n.465G>A
XM_017029165.1:c.600G>A XP_016884654.1:p.Arg200=
NR_169729.1:n.1200G>A
NR_169730.1:n.1103G>A
NR_169731.1:n.432-2449G>A
NR_169732.1:n.254G>A
NR_169733.1:n.312G>A
NR_169734.1:n.336G>A
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