Canonical Allele Identifier: CA197059031

Gene: PTCSC2

Linked Data

• dbSNP Id: rs955328161
• MyVariant Identifiers: chr9:g.100614093G>T (hg19) ; chr9:g.97851811G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851811G>T , CM000671.2:g.97851811G>T	GRCh38
NC_000009.11:g.100614093G>T , CM000671.1:g.100614093G>T	GRCh37
NC_000009.10:g.99653914G>T	NCBI36
NG_011979.1:g.3557G>T

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+1065C>A
XR_930159.1:n.218+1065C>A
XR_930160.1:n.218+1065C>A
XR_930161.1:n.218+1065C>A
NR_147055.1:n.165+1105C>A