Canonical Allele Identifier: CA197059053

Gene: PTCSC2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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