Canonical Allele Identifier: CA1866687867
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786636A= , CM000671.2:g.97786636A= GRCh38
NC_000009.11:g.100548918A= , CM000671.1:g.100548918A= GRCh37
NC_000009.10:g.99588739A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23259T=
NR_147055.1:n.777+17615T=