Canonical Allele Identifier: CA1866666699
Gene: PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97851837G= , CM000671.2:g.97851837G= GRCh38
NC_000009.11:g.100614119G= , CM000671.1:g.100614119G= GRCh37
NC_000009.10:g.99653940G= NCBI36
NG_011979.1:g.3583G=

Transcript Alleles

HGVS Amino-acid change
XR_930158.1:n.218+1039C=
XR_930159.1:n.218+1039C=
XR_930160.1:n.218+1039C=
XR_930161.1:n.218+1039C=
NR_147055.1:n.165+1079C=