Canonical Allele Identifier: CA2528634442
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852309C>A , CM000671.2:g.97852309C>A GRCh38
NC_000009.11:g.100614591C>A , CM000671.1:g.100614591C>A GRCh37
NC_000009.10:g.99654412C>A NCBI36
NG_011979.1:g.4055C>A

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+567G>T
XR_930159.1:n.218+567G>T
XR_930160.1:n.218+567G>T
XR_930161.1:n.218+567G>T
NR_147055.1:n.165+607G>T