Canonical Allele Identifier: CA1866667372
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852069T= , CM000671.2:g.97852069T= GRCh38
NC_000009.11:g.100614351T= , CM000671.1:g.100614351T= GRCh37
NC_000009.10:g.99654172T= NCBI36
NG_011979.1:g.3815T=

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+807A=
XR_930159.1:n.218+807A=
XR_930160.1:n.218+807A=
XR_930161.1:n.218+807A=
NR_147055.1:n.165+847A=