Canonical Allele Identifier: CA513535253
Gene: PPIL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.22012614G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658325G>T , CM000684.2:g.21658325G>T GRCh38
NC_000022.10:g.22012614G>T , CM000684.1:g.22012614G>T GRCh37
NC_000022.9:g.20342614G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.222G>T
ENST00000498589.1:n.402G>T
XM_017029165.1:c.537G>T XP_016884654.1:p.Leu179=
NR_169729.1:n.1137G>T
NR_169730.1:n.1040G>T
NR_169731.1:n.432-2512G>T
NR_169732.1:n.191G>T
NR_169733.1:n.249G>T
NR_169734.1:n.273G>T
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