Canonical Allele Identifier: CA1866666610
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851673T= , CM000671.2:g.97851673T= GRCh38
NC_000009.11:g.100613955T= , CM000671.1:g.100613955T= GRCh37
NC_000009.10:g.99653776T= NCBI36
NG_011979.1:g.3419T=

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+1203A=
XR_930159.1:n.218+1203A=
XR_930160.1:n.218+1203A=
XR_930161.1:n.218+1203A=
NR_147055.1:n.165+1243A=