Canonical Allele Identifier: CA2558680164
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852547A>G , CM000671.2:g.97852547A>G GRCh38
NC_000009.11:g.100614829A>G , CM000671.1:g.100614829A>G GRCh37
NC_000009.10:g.99654650A>G NCBI36
NG_011979.1:g.4293A>G

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+329T>C
XR_930159.1:n.218+329T>C
XR_930160.1:n.218+329T>C
XR_930161.1:n.218+329T>C
NR_147055.1:n.165+369T>C