Canonical Allele Identifier: CA197059087

Gene: PTCSC2

Linked Data

• dbSNP Id: rs948172038
• MyVariant Identifiers: chr9:g.100614447del (hg19) ; chr9:g.97852165del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97852166del , CM000671.2:g.97852166del	GRCh38
NC_000009.11:g.100614448del , CM000671.1:g.100614448del	GRCh37
NC_000009.10:g.99654269del	NCBI36
NG_011979.1:g.3912del

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+711del
XR_930159.1:n.218+711del
XR_930160.1:n.218+711del
XR_930161.1:n.218+711del
NR_147055.1:n.165+751del