Canonical Allele Identifier: CA1866667598
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852262C= , CM000671.2:g.97852262C= GRCh38
NC_000009.11:g.100614544C= , CM000671.1:g.100614544C= GRCh37
NC_000009.10:g.99654365C= NCBI36
NG_011979.1:g.4008C=

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+614G=
XR_930159.1:n.218+614G=
XR_930160.1:n.218+614G=
XR_930161.1:n.218+614G=
NR_147055.1:n.165+654G=