Canonical Allele Identifier: CA1866667839

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1830599916

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97852408_97852410del , CM000671.2:g.97852408_97852410del	GRCh38
NC_000009.11:g.100614690_100614692del , CM000671.1:g.100614690_100614692del	GRCh37
NC_000009.10:g.99654511_99654513del	NCBI36
NG_011979.1:g.4154_4156del

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+474_218+476del
XR_930159.1:n.218+474_218+476del
XR_930160.1:n.218+474_218+476del
XR_930161.1:n.218+474_218+476del
NR_147055.1:n.165+514_165+516del