Canonical Allele Identifier: CA869018906
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1253110138

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851941_97851942insG , CM000671.2:g.97851941_97851942insG GRCh38
NC_000009.11:g.100614223_100614224insG , CM000671.1:g.100614223_100614224insG GRCh37
NC_000009.10:g.99654044_99654045insG NCBI36
NG_011979.1:g.3687_3688insG

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+934_218+935insC
XR_930159.1:n.218+934_218+935insC
XR_930160.1:n.218+934_218+935insC
XR_930161.1:n.218+934_218+935insC
NR_147055.1:n.165+974_165+975insC