Canonical Allele Identifier: CA869018965
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1302110211

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851944_97851945insG , CM000671.2:g.97851944_97851945insG GRCh38
NC_000009.11:g.100614226_100614227insG , CM000671.1:g.100614226_100614227insG GRCh37
NC_000009.10:g.99654047_99654048insG NCBI36
NG_011979.1:g.3690_3691insG

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+931_218+932insC
XR_930159.1:n.218+931_218+932insC
XR_930160.1:n.218+931_218+932insC
XR_930161.1:n.218+931_218+932insC
NR_147055.1:n.165+971_165+972insC