Canonical Allele Identifier: CA869019093
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1293768709

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851949_97851950insG , CM000671.2:g.97851949_97851950insG GRCh38
NC_000009.11:g.100614231_100614232insG , CM000671.1:g.100614231_100614232insG GRCh37
NC_000009.10:g.99654052_99654053insG NCBI36
NG_011979.1:g.3695_3696insG

Transcript Alleles

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