Canonical Allele Identifier: CA2720392152
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs2131483303

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851733A>G , CM000671.2:g.97851733A>G GRCh38
NC_000009.11:g.100614015A>G , CM000671.1:g.100614015A>G GRCh37
NC_000009.10:g.99653836A>G NCBI36
NG_011979.1:g.3479A>G

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+1143T>C
XR_930159.1:n.218+1143T>C
XR_930160.1:n.218+1143T>C
XR_930161.1:n.218+1143T>C
NR_147055.1:n.165+1183T>C