Canonical Allele Identifier: CA1866687882
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1829980805

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786672T>C , CM000671.2:g.97786672T>C GRCh38
NC_000009.11:g.100548954T>C , CM000671.1:g.100548954T>C GRCh37
NC_000009.10:g.99588775T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23223A>G
XR_930162.1:n.7T>C
NR_147055.1:n.777+17579A>G