Canonical Allele Identifier: CA1866691014
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830045380

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97793922T>C , CM000671.2:g.97793922T>C GRCh38
NC_000009.11:g.100556204T>C , CM000671.1:g.100556204T>C GRCh37
NC_000009.10:g.99596025T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+15973A>G
NR_147055.1:n.777+10329A>G