Canonical Allele Identifier: CA1866666707
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830590194

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851845T>C , CM000671.2:g.97851845T>C GRCh38
NC_000009.11:g.100614127T>C , CM000671.1:g.100614127T>C GRCh37
NC_000009.10:g.99653948T>C NCBI36
NG_011979.1:g.3591T>C

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+1031A>G
XR_930159.1:n.218+1031A>G
XR_930160.1:n.218+1031A>G
XR_930161.1:n.218+1031A>G
NR_147055.1:n.165+1071A>G