Canonical Allele Identifier: CA1866687889
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1587786496

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786688C>G , CM000671.2:g.97786688C>G GRCh38
NC_000009.11:g.100548970C>G , CM000671.1:g.100548970C>G GRCh37
NC_000009.10:g.99588791C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23207G>C
XR_930162.1:n.23C>G
NR_147055.1:n.777+17563G>C