Canonical Allele Identifier: CA1127208131
Gene: PTCSC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851935_97851936insGGGGGGGGGGGGGGGGGGGGGGGGGGGG , CM000671.2:g.97851935_97851936insGGGGGGGGGGGGGGGGGGGGGGGGGGGG GRCh38
NC_000009.11:g.100614217_100614218insGGGGGGGGGGGGGGGGGGGGGGGGGGGG , CM000671.1:g.100614217_100614218insGGGGGGGGGGGGGGGGGGGGGGGGGGGG GRCh37
NC_000009.10:g.99654038_99654039insGGGGGGGGGGGGGGGGGGGGGGGGGGGG NCBI36
NG_011979.1:g.3681_3682insGGGGGGGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+942_218+943insCCCCCCCCCCCCCCCCCCCCCCCCCCCC
XR_930159.1:n.218+942_218+943insCCCCCCCCCCCCCCCCCCCCCCCCCCCC
XR_930160.1:n.218+942_218+943insCCCCCCCCCCCCCCCCCCCCCCCCCCCC
XR_930161.1:n.218+942_218+943insCCCCCCCCCCCCCCCCCCCCCCCCCCCC
NR_147055.1:n.165+982_165+983insCCCCCCCCCCCCCCCCCCCCCCCCCCCC