Canonical Allele Identifier: CA1866687872
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1587786484

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97786644T>G , CM000671.2:g.97786644T>G GRCh38
NC_000009.11:g.100548926T>G , CM000671.1:g.100548926T>G GRCh37
NC_000009.10:g.99588747T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930161.1:n.363+23251A>C
NR_147055.1:n.777+17607A>C