Canonical Allele Identifier: CA1866667095
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830594257

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851949_97851950insGCC , CM000671.2:g.97851949_97851950insGCC GRCh38
NC_000009.11:g.100614231_100614232insGCC , CM000671.1:g.100614231_100614232insGCC GRCh37
NC_000009.10:g.99654052_99654053insGCC NCBI36
NG_011979.1:g.3695_3696insGCC

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+928_218+929insCGG
XR_930159.1:n.218+928_218+929insCGG
XR_930160.1:n.218+928_218+929insCGG
XR_930161.1:n.218+928_218+929insCGG
NR_147055.1:n.165+968_165+969insCGG