Canonical Allele Identifier: CA1866668091
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830602899

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852581del , CM000671.2:g.97852581del GRCh38
NC_000009.11:g.100614863del , CM000671.1:g.100614863del GRCh37
NC_000009.10:g.99654684del NCBI36
NG_011979.1:g.4327del

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+298del
XR_930159.1:n.218+298del
XR_930160.1:n.218+298del
XR_930161.1:n.218+298del
NR_147055.1:n.165+338del