Canonical Allele Identifier: CA1127208477
Gene: PTCSC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851950_97851951del , CM000671.2:g.97851950_97851951del GRCh38
NC_000009.11:g.100614232_100614233del , CM000671.1:g.100614232_100614233del GRCh37
NC_000009.10:g.99654053_99654054del NCBI36
NG_011979.1:g.3696_3697del

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+935_218+936del
XR_930159.1:n.218+935_218+936del
XR_930160.1:n.218+935_218+936del
XR_930161.1:n.218+935_218+936del
NR_147055.1:n.165+975_165+976del