Canonical Allele Identifier: CA589532956

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1046408090
• gnomAD v2: 9-100614223-C-A
• gnomAD v3: 9-97851941-C-A
• gnomAD v4: 9-97851941-C-A
• MyVariant Identifiers: chr9:g.100614223C>A (hg19) ; chr9:g.97851941C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851941C>A , CM000671.2:g.97851941C>A	GRCh38
NC_000009.11:g.100614223C>A , CM000671.1:g.100614223C>A	GRCh37
NC_000009.10:g.99654044C>A	NCBI36
NG_011979.1:g.3687C>A

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+935G>T
XR_930159.1:n.218+935G>T
XR_930160.1:n.218+935G>T
XR_930161.1:n.218+935G>T
NR_147055.1:n.165+975G>T