Canonical Allele Identifier: CA1866666741

Gene: PTCSC2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851889_97851891delinsACT , CM000671.2:g.97851889_97851891delinsACT	GRCh38
NC_000009.11:g.100614171_100614173delinsACT , CM000671.1:g.100614171_100614173delinsACT	GRCh37
NC_000009.10:g.99653992_99653994delinsACT	NCBI36
NG_011979.1:g.3635_3637delinsACT

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+985_218+987delinsAGT
XR_930159.1:n.218+985_218+987delinsAGT
XR_930160.1:n.218+985_218+987delinsAGT
XR_930161.1:n.218+985_218+987delinsAGT
NR_147055.1:n.165+1025_165+1027delinsAGT