Canonical Allele Identifier: CA1866667369
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852065A= , CM000671.2:g.97852065A= GRCh38
NC_000009.11:g.100614347A= , CM000671.1:g.100614347A= GRCh37
NC_000009.10:g.99654168A= NCBI36
NG_011979.1:g.3811A=

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+811T=
XR_930159.1:n.218+811T=
XR_930160.1:n.218+811T=
XR_930161.1:n.218+811T=
NR_147055.1:n.165+851T=