Canonical Allele Identifier: CA1866666768
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851905_97851906delinsCA , CM000671.2:g.97851905_97851906delinsCA GRCh38
NC_000009.11:g.100614187_100614188delinsCA , CM000671.1:g.100614187_100614188delinsCA GRCh37
NC_000009.10:g.99654008_99654009delinsCA NCBI36
NG_011979.1:g.3651_3652delinsCA

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+970_218+971delinsTG
XR_930159.1:n.218+970_218+971delinsTG
XR_930160.1:n.218+970_218+971delinsTG
XR_930161.1:n.218+970_218+971delinsTG
NR_147055.1:n.165+1010_165+1011delinsTG