Canonical Allele Identifier: CA1866687908
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786731A= , CM000671.2:g.97786731A= GRCh38
NC_000009.11:g.100549013A= , CM000671.1:g.100549013A= GRCh37
NC_000009.10:g.99588834A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23164T=
XR_930162.1:n.66A=
NR_147055.1:n.777+17520T=