Canonical Allele Identifier: CA197052300
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1001847427

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786636A>G , CM000671.2:g.97786636A>G GRCh38
NC_000009.11:g.100548918A>G , CM000671.1:g.100548918A>G GRCh37
NC_000009.10:g.99588739A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23259T>C
NR_147055.1:n.777+17615T>C