Canonical Allele Identifier: CA1866690922
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97793719_97793720delinsAG , CM000671.2:g.97793719_97793720delinsAG GRCh38
NC_000009.11:g.100556001_100556002delinsAG , CM000671.1:g.100556001_100556002delinsAG GRCh37
NC_000009.10:g.99595822_99595823delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930161.1:n.363+16175_363+16176delinsCT
XR_930162.1:n.6404_6405delinsAG
NR_147055.1:n.777+10531_777+10532delinsCT