Canonical Allele Identifier: CA1866690956
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97793795G= , CM000671.2:g.97793795G= GRCh38
NC_000009.11:g.100556077G= , CM000671.1:g.100556077G= GRCh37
NC_000009.10:g.99595898G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930161.1:n.363+16100C=
XR_930162.1:n.6480G=
NR_147055.1:n.777+10456C=