Canonical Allele Identifier: CA1866690935
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97793736G= , CM000671.2:g.97793736G= GRCh38
NC_000009.11:g.100556018G= , CM000671.1:g.100556018G= GRCh37
NC_000009.10:g.99595839G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930161.1:n.363+16159C=
XR_930162.1:n.6421G=
NR_147055.1:n.777+10515C=