Canonical Allele Identifier: CA1866668051
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852538_97852539delinsAC , CM000671.2:g.97852538_97852539delinsAC GRCh38
NC_000009.11:g.100614820_100614821delinsAC , CM000671.1:g.100614820_100614821delinsAC GRCh37
NC_000009.10:g.99654641_99654642delinsAC NCBI36
NG_011979.1:g.4284_4285delinsAC

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+337_218+338delinsGT
XR_930159.1:n.218+337_218+338delinsGT
XR_930160.1:n.218+337_218+338delinsGT
XR_930161.1:n.218+337_218+338delinsGT
NR_147055.1:n.165+377_165+378delinsGT