Canonical Allele Identifier: CA1866666675
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851792_97851793delinsAG , CM000671.2:g.97851792_97851793delinsAG GRCh38
NC_000009.11:g.100614074_100614075delinsAG , CM000671.1:g.100614074_100614075delinsAG GRCh37
NC_000009.10:g.99653895_99653896delinsAG NCBI36
NG_011979.1:g.3538_3539delinsAG

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+1083_218+1084delinsCT
XR_930159.1:n.218+1083_218+1084delinsCT
XR_930160.1:n.218+1083_218+1084delinsCT
XR_930161.1:n.218+1083_218+1084delinsCT
NR_147055.1:n.165+1123_165+1124delinsCT