Canonical Allele Identifier: CA1866666975
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1244295370

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851940_97851941insAA , CM000671.2:g.97851940_97851941insAA GRCh38
NC_000009.11:g.100614222_100614223insAA , CM000671.1:g.100614222_100614223insAA GRCh37
NC_000009.10:g.99654043_99654044insAA NCBI36
NG_011979.1:g.3686_3687insAA

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+935_218+936insTT
XR_930159.1:n.218+935_218+936insTT
XR_930160.1:n.218+935_218+936insTT
XR_930161.1:n.218+935_218+936insTT
NR_147055.1:n.165+975_165+976insTT