Canonical Allele Identifier: CA869019233
Gene: PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1449340491

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852061dup , CM000671.2:g.97852061dup GRCh38
NC_000009.11:g.100614343dup , CM000671.1:g.100614343dup GRCh37
NC_000009.10:g.99654164dup NCBI36
NG_011979.1:g.3807dup

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+817dup
XR_930159.1:n.218+817dup
XR_930160.1:n.218+817dup
XR_930161.1:n.218+817dup
NR_147055.1:n.165+857dup