Canonical Allele Identifier: CA1866666850
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830592361

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851935_97851936insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG , CM000671.2:g.97851935_97851936insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG GRCh38
NC_000009.11:g.100614217_100614218insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG , CM000671.1:g.100614217_100614218insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG GRCh37
NC_000009.10:g.99654038_99654039insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG NCBI36
NG_011979.1:g.3681_3682insGGGGGGGGGGGGGGGGGGGGGGGGGGGGGG

Transcript Alleles

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