Canonical Allele Identifier: CA1127208565
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830594086

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851948_97851949insGCC , CM000671.2:g.97851948_97851949insGCC GRCh38
NC_000009.11:g.100614230_100614231insGCC , CM000671.1:g.100614230_100614231insGCC GRCh37
NC_000009.10:g.99654051_99654052insGCC NCBI36
NG_011979.1:g.3694_3695insGCC

Transcript Alleles

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