Canonical Allele Identifier: CA2655514838
Gene: PPIL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658489A>T , CM000684.2:g.21658489A>T GRCh38
NC_000022.10:g.22012778A>T , CM000684.1:g.22012778A>T GRCh37
NC_000022.9:g.20342778A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641967.1:n.286+100A>T
ENST00000498589.1:n.539+27A>T
XM_017029165.1:c.674+27A>T XP_016884654.1:n.674+27A>T
NR_169729.1:n.1301A>T
NR_169730.1:n.1204A>T
NR_169731.1:n.432-2348A>T
NR_169732.1:n.328+27A>T
NR_169733.1:n.386+27A>T
NR_169734.1:n.410+27A>T