Canonical Allele Identifier: CA1866687883
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786674T= , CM000671.2:g.97786674T= GRCh38
NC_000009.11:g.100548956T= , CM000671.1:g.100548956T= GRCh37
NC_000009.10:g.99588777T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23221A=
XR_930162.1:n.9T=
NR_147055.1:n.777+17577A=