Canonical Allele Identifier: CA1866690968
Gene: PTCSC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97793821A= , CM000671.2:g.97793821A= GRCh38
NC_000009.11:g.100556103A= , CM000671.1:g.100556103A= GRCh37
NC_000009.10:g.99595924A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930161.1:n.363+16074T=
XR_930162.1:n.6506A=
NR_147055.1:n.777+10430T=
Search 100 bp 5'
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