Canonical Allele Identifier: CA2655514829
Gene: PPIL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658487G>T , CM000684.2:g.21658487G>T GRCh38
NC_000022.10:g.22012776G>T , CM000684.1:g.22012776G>T GRCh37
NC_000022.9:g.20342776G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641967.1:n.286+98G>T
ENST00000498589.1:n.539+25G>T
XM_017029165.1:c.674+25G>T XP_016884654.1:n.674+25G>T
NR_169729.1:n.1299G>T
NR_169730.1:n.1202G>T
NR_169731.1:n.432-2350G>T
NR_169732.1:n.328+25G>T
NR_169733.1:n.386+25G>T
NR_169734.1:n.410+25G>T