Canonical Allele Identifier: CA1866691351
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97794690A= , CM000671.2:g.97794690A= GRCh38
NC_000009.11:g.100556972A= , CM000671.1:g.100556972A= GRCh37
NC_000009.10:g.99596793A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930161.1:n.363+15205T=
NR_147055.1:n.777+9561T=