Canonical Allele Identifier: CA1866667007
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851944C= , CM000671.2:g.97851944C= GRCh38
NC_000009.11:g.100614226C= , CM000671.1:g.100614226C= GRCh37
NC_000009.10:g.99654047C= NCBI36
NG_011979.1:g.3690C=

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+932G=
XR_930159.1:n.218+932G=
XR_930160.1:n.218+932G=
XR_930161.1:n.218+932G=
NR_147055.1:n.165+972G=