Canonical Allele Identifier: CA2785233579
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851936_97851937insGGGGGGGG , CM000671.2:g.97851936_97851937insGGGGGGGG GRCh38
NC_000009.11:g.100614218_100614219insGGGGGGGG , CM000671.1:g.100614218_100614219insGGGGGGGG GRCh37
NC_000009.10:g.99654039_99654040insGGGGGGGG NCBI36
NG_011979.1:g.3682_3683insGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+939_218+940insCCCCCCCC
XR_930159.1:n.218+939_218+940insCCCCCCCC
XR_930160.1:n.218+939_218+940insCCCCCCCC
XR_930161.1:n.218+939_218+940insCCCCCCCC
NR_147055.1:n.165+979_165+980insCCCCCCCC