Canonical Allele Identifier: CA1866666676
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851793G= , CM000671.2:g.97851793G= GRCh38
NC_000009.11:g.100614075G= , CM000671.1:g.100614075G= GRCh37
NC_000009.10:g.99653896G= NCBI36
NG_011979.1:g.3539G=

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+1083C=
XR_930159.1:n.218+1083C=
XR_930160.1:n.218+1083C=
XR_930161.1:n.218+1083C=
NR_147055.1:n.165+1123C=