Canonical Allele Identifier: CA1127208463
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830592886

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851939del , CM000671.2:g.97851939del GRCh38
NC_000009.11:g.100614221del , CM000671.1:g.100614221del GRCh37
NC_000009.10:g.99654042del NCBI36
NG_011979.1:g.3685del

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+937del
XR_930159.1:n.218+937del
XR_930160.1:n.218+937del
XR_930161.1:n.218+937del
NR_147055.1:n.165+977del