Canonical Allele Identifier: CA13034679
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97787746T>C , CM000671.2:g.97787746T>C GRCh38
NC_000009.11:g.100550028T>C , CM000671.1:g.100550028T>C GRCh37
NC_000009.10:g.99589849T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930161.1:n.363+22149A>G
XR_930162.1:n.431T>C
NR_147055.1:n.777+16505A>G