Canonical Allele Identifier: CA589532943
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs34618971

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+936del
XR_930159.1:n.218+936del
XR_930160.1:n.218+936del
XR_930161.1:n.218+936del
NR_147055.1:n.165+976del