Canonical Allele Identifier: CA918516231

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1406003437

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851932_97851933dup , CM000671.2:g.97851932_97851933dup	GRCh38
NC_000009.11:g.100614214_100614215dup , CM000671.1:g.100614214_100614215dup	GRCh37
NC_000009.10:g.99654035_99654036dup	NCBI36
NG_011979.1:g.3678_3679dup

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+945_218+946dup
XR_930159.1:n.218+945_218+946dup
XR_930160.1:n.218+945_218+946dup
XR_930161.1:n.218+945_218+946dup
NR_147055.1:n.165+985_165+986dup