Canonical Allele Identifier: CA513535469
Gene: PPIL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.22012684G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658395G>T , CM000684.2:g.21658395G>T GRCh38
NC_000022.10:g.22012684G>T , CM000684.1:g.22012684G>T GRCh37
NC_000022.9:g.20342684G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+6G>T
ENST00000498589.1:n.472G>T
XM_017029165.1:c.607G>T XP_016884654.1:p.Asp203Tyr
NR_169729.1:n.1207G>T
NR_169730.1:n.1110G>T
NR_169731.1:n.432-2442G>T
NR_169732.1:n.261G>T
NR_169733.1:n.319G>T
NR_169734.1:n.343G>T