Canonical Allele Identifier: CA1866667131
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1554712836

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851951_97851952insCGCC , CM000671.2:g.97851951_97851952insCGCC GRCh38
NC_000009.11:g.100614233_100614234insCGCC , CM000671.1:g.100614233_100614234insCGCC GRCh37
NC_000009.10:g.99654054_99654055insCGCC NCBI36
NG_011979.1:g.3697_3698insCGCC

Transcript Alleles

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