Canonical Allele Identifier: CA869018797

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1187848370
• gnomAD v3: 9-97851877-G-A
• gnomAD v4: 9-97851877-G-A
• MyVariant Identifiers: chr9:g.100614159G>A (hg19) ; chr9:g.97851877G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851877G>A , CM000671.2:g.97851877G>A	GRCh38
NC_000009.11:g.100614159G>A , CM000671.1:g.100614159G>A	GRCh37
NC_000009.10:g.99653980G>A	NCBI36
NG_011979.1:g.3623G>A

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+999C>T
XR_930159.1:n.218+999C>T
XR_930160.1:n.218+999C>T
XR_930161.1:n.218+999C>T
NR_147055.1:n.165+1039C>T