Canonical Allele Identifier: CA2655514328
Gene: PPIL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658247T>C , CM000684.2:g.21658247T>C GRCh38
NC_000022.10:g.22012536T>C , CM000684.1:g.22012536T>C GRCh37
NC_000022.9:g.20342536T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.163-19T>C
ENST00000498589.1:n.343-19T>C
XM_017029165.1:c.478-19T>C XP_016884654.1:n.478-19T>C
NR_169729.1:n.1059T>C
NR_169730.1:n.962T>C
NR_169731.1:n.432-2590T>C
NR_169732.1:n.132-19T>C
NR_169733.1:n.214-43T>C
NR_169734.1:n.214-19T>C