Canonical Allele Identifier: CA589533011
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1554712868

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852064_97852065del , CM000671.2:g.97852064_97852065del GRCh38
NC_000009.11:g.100614346_100614347del , CM000671.1:g.100614346_100614347del GRCh37
NC_000009.10:g.99654167_99654168del NCBI36
NG_011979.1:g.3810_3811del

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+812_218+813del
XR_930159.1:n.218+812_218+813del
XR_930160.1:n.218+812_218+813del
XR_930161.1:n.218+812_218+813del
NR_147055.1:n.165+852_165+853del