Canonical Allele Identifier: CA513535476
Gene: PPIL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.22012686T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21658397T>C , CM000684.2:g.21658397T>C GRCh38
NC_000022.10:g.22012686T>C , CM000684.1:g.22012686T>C GRCh37
NC_000022.9:g.20342686T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000641967.1:n.286+8T>C
ENST00000498589.1:n.474T>C
XM_017029165.1:c.609T>C XP_016884654.1:p.Asp203=
NR_169729.1:n.1209T>C
NR_169730.1:n.1112T>C
NR_169731.1:n.432-2440T>C
NR_169732.1:n.263T>C
NR_169733.1:n.321T>C
NR_169734.1:n.345T>C