Canonical Allele Identifier: CA1866690957
Gene: PTCSC2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97793800T= , CM000671.2:g.97793800T= GRCh38
NC_000009.11:g.100556082T= , CM000671.1:g.100556082T= GRCh37
NC_000009.10:g.99595903T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930161.1:n.363+16095A=
XR_930162.1:n.6485T=
NR_147055.1:n.777+10451A=
Search 100 bp 5'
Search 100 bp 3'