Canonical Allele Identifier: CA1127208972
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830602424

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852539del , CM000671.2:g.97852539del GRCh38
NC_000009.11:g.100614821del , CM000671.1:g.100614821del GRCh37
NC_000009.10:g.99654642del NCBI36
NG_011979.1:g.4285del

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+337del
XR_930159.1:n.218+337del
XR_930160.1:n.218+337del
XR_930161.1:n.218+337del
NR_147055.1:n.165+377del