Canonical Allele Identifier: CA1866667894
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852425T= , CM000671.2:g.97852425T= GRCh38
NC_000009.11:g.100614707T= , CM000671.1:g.100614707T= GRCh37
NC_000009.10:g.99654528T= NCBI36
NG_011979.1:g.4171T=

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+451A=
XR_930159.1:n.218+451A=
XR_930160.1:n.218+451A=
XR_930161.1:n.218+451A=
NR_147055.1:n.165+491A=