Canonical Allele Identifier: CA1866667128

Gene: PTCSC2

Linked Data

• dbSNP Id: rs1293768709

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97851949_97851950insA , CM000671.2:g.97851949_97851950insA	GRCh38
NC_000009.11:g.100614231_100614232insA , CM000671.1:g.100614231_100614232insA	GRCh37
NC_000009.10:g.99654052_99654053insA	NCBI36
NG_011979.1:g.3695_3696insA

Transcript Alleles

HGVS	Amino-acid Change
XR_930158.1:n.218+926_218+927insT
XR_930159.1:n.218+926_218+927insT
XR_930160.1:n.218+926_218+927insT
XR_930161.1:n.218+926_218+927insT
NR_147055.1:n.165+966_165+967insT