Canonical Allele Identifier: CA1866690960
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97793802A= , CM000671.2:g.97793802A= GRCh38
NC_000009.11:g.100556084A= , CM000671.1:g.100556084A= GRCh37
NC_000009.10:g.99595905A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930161.1:n.363+16093T=
XR_930162.1:n.6487A=
NR_147055.1:n.777+10449T=