Canonical Allele Identifier: CA653192396
Gene: PTCSC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786665G>A , CM000671.2:g.97786665G>A GRCh38
NC_000009.11:g.100548947G>A , CM000671.1:g.100548947G>A GRCh37
NC_000009.10:g.99588768G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23230C>T
NR_147055.1:n.777+17586C>T