Canonical Allele Identifier: CA1866666964
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830593355

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851943_97851944insGCCC , CM000671.2:g.97851943_97851944insGCCC GRCh38
NC_000009.11:g.100614225_100614226insGCCC , CM000671.1:g.100614225_100614226insGCCC GRCh37
NC_000009.10:g.99654046_99654047insGCCC NCBI36
NG_011979.1:g.3689_3690insGCCC

Transcript Alleles

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