Canonical Allele Identifier: CA1866687885
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1829980838

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786679C>T , CM000671.2:g.97786679C>T GRCh38
NC_000009.11:g.100548961C>T , CM000671.1:g.100548961C>T GRCh37
NC_000009.10:g.99588782C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23216G>A
XR_930162.1:n.14C>T
NR_147055.1:n.777+17572G>A