Canonical Allele Identifier: CA1866667338
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852051A= , CM000671.2:g.97852051A= GRCh38
NC_000009.11:g.100614333A= , CM000671.1:g.100614333A= GRCh37
NC_000009.10:g.99654154A= NCBI36
NG_011979.1:g.3797A=

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+825T=
XR_930159.1:n.218+825T=
XR_930160.1:n.218+825T=
XR_930161.1:n.218+825T=
NR_147055.1:n.165+865T=