Canonical Allele Identifier: CA1866666743

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1830590972

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851891_97851892del , CM000671.2:g.97851891_97851892del	GRCh38
NC_000009.11:g.100614173_100614174del , CM000671.1:g.100614173_100614174del	GRCh37
NC_000009.10:g.99653994_99653995del	NCBI36
NG_011979.1:g.3637_3638del

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+985_218+986del
XR_930159.1:n.218+985_218+986del
XR_930160.1:n.218+985_218+986del
XR_930161.1:n.218+985_218+986del
NR_147055.1:n.165+1025_165+1026del