Canonical Allele Identifier: CA1127208515
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1554712818

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851943_97851944insG , CM000671.2:g.97851943_97851944insG GRCh38
NC_000009.11:g.100614225_100614226insG , CM000671.1:g.100614225_100614226insG GRCh37
NC_000009.10:g.99654046_99654047insG NCBI36
NG_011979.1:g.3689_3690insG

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+932_218+933insC
XR_930159.1:n.218+932_218+933insC
XR_930160.1:n.218+932_218+933insC
XR_930161.1:n.218+932_218+933insC
NR_147055.1:n.165+972_165+973insC