Canonical Allele Identifier: CA2655514896
Gene: PPIL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658525G>T , CM000684.2:g.21658525G>T GRCh38
NC_000022.10:g.22012814G>T , CM000684.1:g.22012814G>T GRCh37
NC_000022.9:g.20342814G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+136G>T
ENST00000498589.1:n.539+63G>T
XM_017029165.1:c.674+63G>T XP_016884654.1:n.674+63G>T
NR_169729.1:n.1337G>T
NR_169730.1:n.1240G>T
NR_169731.1:n.432-2312G>T
NR_169732.1:n.328+63G>T
NR_169733.1:n.386+63G>T
NR_169734.1:n.410+63G>T