Canonical Allele Identifier: CA653191706
Gene: PTCSC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852319_97852320insA , CM000671.2:g.97852319_97852320insA GRCh38
NC_000009.11:g.100614601_100614602insA , CM000671.1:g.100614601_100614602insA GRCh37
NC_000009.10:g.99654422_99654423insA NCBI36
NG_011979.1:g.4065_4066insA

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+556_218+557insT
XR_930159.1:n.218+556_218+557insT
XR_930160.1:n.218+556_218+557insT
XR_930161.1:n.218+556_218+557insT
NR_147055.1:n.165+596_165+597insT