Canonical Allele Identifier: CA1127208656
Gene: PTCSC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851956dup , CM000671.2:g.97851956dup GRCh38
NC_000009.11:g.100614238dup , CM000671.1:g.100614238dup GRCh37
NC_000009.10:g.99654059dup NCBI36
NG_011979.1:g.3702dup

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+923dup
XR_930159.1:n.218+923dup
XR_930160.1:n.218+923dup
XR_930161.1:n.218+923dup
NR_147055.1:n.165+963dup