Canonical Allele Identifier: CA589532972

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1554712826
• gnomAD v2: 9-100614228-C-CA
• gnomAD v3: 9-97851946-C-CA
• gnomAD v4: 9-97851946-C-CA
• MyVariant Identifiers: chr9:g.100614228_100614229insA (hg19) ; chr9:g.97851946_97851947insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851946_97851947insA , CM000671.2:g.97851946_97851947insA	GRCh38
NC_000009.11:g.100614228_100614229insA , CM000671.1:g.100614228_100614229insA	GRCh37
NC_000009.10:g.99654049_99654050insA	NCBI36
NG_011979.1:g.3692_3693insA

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+929_218+930insT
XR_930159.1:n.218+929_218+930insT
XR_930160.1:n.218+929_218+930insT
XR_930161.1:n.218+929_218+930insT
NR_147055.1:n.165+969_165+970insT