Canonical Allele Identifier: CA2846498149
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851939_97851940insGGCCCCCCGC , CM000671.2:g.97851939_97851940insGGCCCCCCGC GRCh38
NC_000009.11:g.100614221_100614222insGGCCCCCCGC , CM000671.1:g.100614221_100614222insGGCCCCCCGC GRCh37
NC_000009.10:g.99654042_99654043insGGCCCCCCGC NCBI36
NG_011979.1:g.3685_3686insGGCCCCCCGC

Transcript Alleles

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