Canonical Allele Identifier: CA2655514851
Gene: PPIL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658496C>T , CM000684.2:g.21658496C>T GRCh38
NC_000022.10:g.22012785C>T , CM000684.1:g.22012785C>T GRCh37
NC_000022.9:g.20342785C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000641967.1:n.286+107C>T
ENST00000498589.1:n.539+34C>T
XM_017029165.1:c.674+34C>T XP_016884654.1:n.674+34C>T
NR_169729.1:n.1308C>T
NR_169730.1:n.1211C>T
NR_169731.1:n.432-2341C>T
NR_169732.1:n.328+34C>T
NR_169733.1:n.386+34C>T
NR_169734.1:n.410+34C>T