Canonical Allele Identifier: CA1866666748

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1830591047

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851892C>G , CM000671.2:g.97851892C>G	GRCh38
NC_000009.11:g.100614174C>G , CM000671.1:g.100614174C>G	GRCh37
NC_000009.10:g.99653995C>G	NCBI36
NG_011979.1:g.3638C>G

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+984G>C
XR_930159.1:n.218+984G>C
XR_930160.1:n.218+984G>C
XR_930161.1:n.218+984G>C
NR_147055.1:n.165+1024G>C