Canonical Allele Identifier: CA1866667902
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852448_97852449delinsAT , CM000671.2:g.97852448_97852449delinsAT GRCh38
NC_000009.11:g.100614730_100614731delinsAT , CM000671.1:g.100614730_100614731delinsAT GRCh37
NC_000009.10:g.99654551_99654552delinsAT NCBI36
NG_011979.1:g.4194_4195delinsAT

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+427_218+428delinsAT
XR_930159.1:n.218+427_218+428delinsAT
XR_930160.1:n.218+427_218+428delinsAT
XR_930161.1:n.218+427_218+428delinsAT
NR_147055.1:n.165+467_165+468delinsAT