Canonical Allele Identifier: CA1866690959
Gene: PTCSC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97793801G= , CM000671.2:g.97793801G= GRCh38
NC_000009.11:g.100556083G= , CM000671.1:g.100556083G= GRCh37
NC_000009.10:g.99595904G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930161.1:n.363+16094C=
XR_930162.1:n.6486G=
NR_147055.1:n.777+10450C=
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