Canonical Allele Identifier: CA1127208562
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1554712826

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851946_97851947insT , CM000671.2:g.97851946_97851947insT GRCh38
NC_000009.11:g.100614228_100614229insT , CM000671.1:g.100614228_100614229insT GRCh37
NC_000009.10:g.99654049_99654050insT NCBI36
NG_011979.1:g.3692_3693insT

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+929_218+930insA
XR_930159.1:n.218+929_218+930insA
XR_930160.1:n.218+929_218+930insA
XR_930161.1:n.218+929_218+930insA
NR_147055.1:n.165+969_165+970insA