Canonical Allele Identifier: CA869002476
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs7864322

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786652C>G , CM000671.2:g.97786652C>G GRCh38
NC_000009.11:g.100548934C>G , CM000671.1:g.100548934C>G GRCh37
NC_000009.10:g.99588755C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23243G>C
NR_147055.1:n.777+17599G>C