Canonical Allele Identifier: CA589532985
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1293768709

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851949_97851950insT , CM000671.2:g.97851949_97851950insT GRCh38
NC_000009.11:g.100614231_100614232insT , CM000671.1:g.100614231_100614232insT GRCh37
NC_000009.10:g.99654052_99654053insT NCBI36
NG_011979.1:g.3695_3696insT

Transcript Alleles

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