Canonical Allele Identifier: CA1127208493
Gene: PTCSC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851941_97851942insAC , CM000671.2:g.97851941_97851942insAC GRCh38
NC_000009.11:g.100614223_100614224insAC , CM000671.1:g.100614223_100614224insAC GRCh37
NC_000009.10:g.99654044_99654045insAC NCBI36
NG_011979.1:g.3687_3688insAC

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+935_218+936insTG
XR_930159.1:n.218+935_218+936insTG
XR_930160.1:n.218+935_218+936insTG
XR_930161.1:n.218+935_218+936insTG
NR_147055.1:n.165+975_165+976insTG