Canonical Allele Identifier: CA1866667025

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1830593778

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851946_97851947insTCC , CM000671.2:g.97851946_97851947insTCC	GRCh38
NC_000009.11:g.100614228_100614229insTCC , CM000671.1:g.100614228_100614229insTCC	GRCh37
NC_000009.10:g.99654049_99654050insTCC	NCBI36
NG_011979.1:g.3692_3693insTCC

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+931_218+932insAGG
XR_930159.1:n.218+931_218+932insAGG
XR_930160.1:n.218+931_218+932insAGG
XR_930161.1:n.218+931_218+932insAGG
NR_147055.1:n.165+971_165+972insAGG