Canonical Allele Identifier: CA1866691012
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1564075635

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97793916A>G , CM000671.2:g.97793916A>G GRCh38
NC_000009.11:g.100556198A>G , CM000671.1:g.100556198A>G GRCh37
NC_000009.10:g.99596019A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930161.1:n.363+15979T>C
NR_147055.1:n.777+10335T>C