Canonical Allele Identifier: CA197059161

Gene: PTCSC2

Linked Data

• dbSNP Id: rs35241326
• MyVariant Identifiers: chr9:g.100615049del (hg19) ; chr9:g.97852767del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97852768del , CM000671.2:g.97852768del	GRCh38
NC_000009.11:g.100615050del , CM000671.1:g.100615050del	GRCh37
NC_000009.10:g.99654871del	NCBI36
NG_011979.1:g.4514del

Transcript Alleles

HGVS	Amino-acid change
XR_930158.1:n.218+109del
XR_930159.1:n.218+109del
XR_930160.1:n.218+109del
XR_930161.1:n.218+109del
NR_147055.1:n.165+149del