Canonical Allele Identifier: CA513535498
Gene: PPIL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.22012692T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658403T>G , CM000684.2:g.21658403T>G GRCh38
NC_000022.10:g.22012692T>G , CM000684.1:g.22012692T>G GRCh37
NC_000022.9:g.20342692T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+14T>G
ENST00000498589.1:n.480T>G
XM_017029165.1:c.615T>G XP_016884654.1:p.Pro205=
NR_169729.1:n.1215T>G
NR_169730.1:n.1118T>G
NR_169731.1:n.432-2434T>G
NR_169732.1:n.269T>G
NR_169733.1:n.327T>G
NR_169734.1:n.351T>G