Canonical Allele Identifier: CA1866666984
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830593456

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851943_97851944insGCC , CM000671.2:g.97851943_97851944insGCC GRCh38
NC_000009.11:g.100614225_100614226insGCC , CM000671.1:g.100614225_100614226insGCC GRCh37
NC_000009.10:g.99654046_99654047insGCC NCBI36
NG_011979.1:g.3689_3690insGCC

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+934_218+935insCGG
XR_930159.1:n.218+934_218+935insCGG
XR_930160.1:n.218+934_218+935insCGG
XR_930161.1:n.218+934_218+935insCGG
NR_147055.1:n.165+974_165+975insCGG