Canonical Allele Identifier: CA1866686861
Community Standard Title: NC_000009.12:g.97784318C=
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97784318C= , CM000671.2:g.97784318C= GRCh38
NC_000009.11:g.100546600C= , CM000671.1:g.100546600C= GRCh37
NC_000009.10:g.99586421C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_147055.1:n.777+19933G=
XR_930161.1:n.363+25577G=