Canonical Allele Identifier: CA869004621

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1199612314
• gnomAD v3: 9-97793926-C-T
• gnomAD v4: 9-97793926-C-T
• MyVariant Identifiers: chr9:g.100556208C>T (hg19) ; chr9:g.97793926C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97793926C>T , CM000671.2:g.97793926C>T	GRCh38
NC_000009.11:g.100556208C>T , CM000671.1:g.100556208C>T	GRCh37
NC_000009.10:g.99596029C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930161.1:n.363+15969G>A
NR_147055.1:n.777+10325G>A