Canonical Allele Identifier: CA869018959

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1554712821
• MyVariant Identifiers: chr9:g.100614226_100614227insCG (hg19) ; chr9:g.97851944_97851945insCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851945_97851946insGC , CM000671.2:g.97851945_97851946insGC	GRCh38
NC_000009.11:g.100614227_100614228insGC , CM000671.1:g.100614227_100614228insGC	GRCh37
NC_000009.10:g.99654048_99654049insGC	NCBI36
NG_011979.1:g.3691_3692insGC

Transcript Alleles

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