Canonical Allele Identifier: CA1866687893
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1829980960

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786693G>A , CM000671.2:g.97786693G>A GRCh38
NC_000009.11:g.100548975G>A , CM000671.1:g.100548975G>A GRCh37
NC_000009.10:g.99588796G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23202C>T
XR_930162.1:n.28G>A
NR_147055.1:n.777+17558C>T