Canonical Allele Identifier: CA1127208354
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs66806500

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851938del , CM000671.2:g.97851938del GRCh38
NC_000009.11:g.100614220del , CM000671.1:g.100614220del GRCh37
NC_000009.10:g.99654041del NCBI36
NG_011979.1:g.3684del

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+940del
XR_930159.1:n.218+940del
XR_930160.1:n.218+940del
XR_930161.1:n.218+940del
NR_147055.1:n.165+980del