Canonical Allele Identifier: CA197052299
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs957481875

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786631C>T , CM000671.2:g.97786631C>T GRCh38
NC_000009.11:g.100548913C>T , CM000671.1:g.100548913C>T GRCh37
NC_000009.10:g.99588734C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23264G>A
NR_147055.1:n.777+17620G>A