Canonical Allele Identifier: CA1866667577
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97852247C= , CM000671.2:g.97852247C= GRCh38
NC_000009.11:g.100614529C= , CM000671.1:g.100614529C= GRCh37
NC_000009.10:g.99654350C= NCBI36
NG_011979.1:g.3993C=

Transcript Alleles

HGVS Amino-acid Change
XR_930158.1:n.218+629G=
XR_930159.1:n.218+629G=
XR_930160.1:n.218+629G=
XR_930161.1:n.218+629G=
NR_147055.1:n.165+669G=