Canonical Allele Identifier: CA1866690980
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97793837A= , CM000671.2:g.97793837A= GRCh38
NC_000009.11:g.100556119A= , CM000671.1:g.100556119A= GRCh37
NC_000009.10:g.99595940A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930161.1:n.363+16058T=
XR_930162.1:n.6522A=
NR_147055.1:n.777+10414T=