Canonical Allele Identifier: CA1866667196
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851970_97851971delinsCG , CM000671.2:g.97851970_97851971delinsCG GRCh38
NC_000009.11:g.100614252_100614253delinsCG , CM000671.1:g.100614252_100614253delinsCG GRCh37
NC_000009.10:g.99654073_99654074delinsCG NCBI36
NG_011979.1:g.3716_3717delinsCG

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+905_218+906delinsCG
XR_930159.1:n.218+905_218+906delinsCG
XR_930160.1:n.218+905_218+906delinsCG
XR_930161.1:n.218+905_218+906delinsCG
NR_147055.1:n.165+945_165+946delinsCG