Canonical Allele Identifier: CA1866666812
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1830591977

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851928del , CM000671.2:g.97851928del GRCh38
NC_000009.11:g.100614210del , CM000671.1:g.100614210del GRCh37
NC_000009.10:g.99654031del NCBI36
NG_011979.1:g.3674del

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+948del
XR_930159.1:n.218+948del
XR_930160.1:n.218+948del
XR_930161.1:n.218+948del
NR_147055.1:n.165+988del