Canonical Allele Identifier: CA1866666949
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830593145

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851940_97851941insTC , CM000671.2:g.97851940_97851941insTC GRCh38
NC_000009.11:g.100614222_100614223insTC , CM000671.1:g.100614222_100614223insTC GRCh37
NC_000009.10:g.99654043_99654044insTC NCBI36
NG_011979.1:g.3686_3687insTC

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+936_218+937insAG
XR_930159.1:n.218+936_218+937insAG
XR_930160.1:n.218+936_218+937insAG
XR_930161.1:n.218+936_218+937insAG
NR_147055.1:n.165+976_165+977insAG