Canonical Allele Identifier: CA197059056

Gene: PTCSC2

Linked Data

• dbSNP Id: rs994434091
• gnomAD v2: 9-100614227-C-G
• gnomAD v3: 9-97851945-C-G
• gnomAD v4: 9-97851945-C-G
• MyVariant Identifiers: chr9:g.100614227C>G (hg19) ; chr9:g.97851945C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851945C>G , CM000671.2:g.97851945C>G	GRCh38
NC_000009.11:g.100614227C>G , CM000671.1:g.100614227C>G	GRCh37
NC_000009.10:g.99654048C>G	NCBI36
NG_011979.1:g.3691C>G

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+931G>C
XR_930159.1:n.218+931G>C
XR_930160.1:n.218+931G>C
XR_930161.1:n.218+931G>C
NR_147055.1:n.165+971G>C