Canonical Allele Identifier: CA1866687888
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786688C= , CM000671.2:g.97786688C= GRCh38
NC_000009.11:g.100548970C= , CM000671.1:g.100548970C= GRCh37
NC_000009.10:g.99588791C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23207G=
XR_930162.1:n.23C=
NR_147055.1:n.777+17563G=