Canonical Allele Identifier: CA1866687866
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786634T= , CM000671.2:g.97786634T= GRCh38
NC_000009.11:g.100548916T= , CM000671.1:g.100548916T= GRCh37
NC_000009.10:g.99588737T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23261A=
NR_147055.1:n.777+17617A=