Canonical Allele Identifier: CA1866690939
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97793750G= , CM000671.2:g.97793750G= GRCh38
NC_000009.11:g.100556032G= , CM000671.1:g.100556032G= GRCh37
NC_000009.10:g.99595853G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930161.1:n.363+16145C=
XR_930162.1:n.6435G=
NR_147055.1:n.777+10501C=