Canonical Allele Identifier: CA1866666650
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851753G= , CM000671.2:g.97851753G= GRCh38
NC_000009.11:g.100614035G= , CM000671.1:g.100614035G= GRCh37
NC_000009.10:g.99653856G= NCBI36
NG_011979.1:g.3499G=

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+1123C=
XR_930159.1:n.218+1123C=
XR_930160.1:n.218+1123C=
XR_930161.1:n.218+1123C=
NR_147055.1:n.165+1163C=