Canonical Allele Identifier: CA1866690995
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830045114

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97793888G>A , CM000671.2:g.97793888G>A GRCh38
NC_000009.11:g.100556170G>A , CM000671.1:g.100556170G>A GRCh37
NC_000009.10:g.99595991G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+16007C>T
NR_147055.1:n.777+10363C>T