Canonical Allele Identifier: CA513535474
Gene: PPIL2 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000641967.1:n.286+8T>G
ENST00000498589.1:n.474T>G
XM_017029165.1:c.609T>G XP_016884654.1:p.Asp203Glu
NR_169729.1:n.1209T>G
NR_169730.1:n.1112T>G
NR_169731.1:n.432-2440T>G
NR_169732.1:n.263T>G
NR_169733.1:n.321T>G
NR_169734.1:n.345T>G