Canonical Allele Identifier: CA2002576378
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116442779C= , CM000673.2:g.116442779C= GRCh38
NC_000011.9:g.116313496C= , CM000673.1:g.116313496C= GRCh37
NC_000011.8:g.115818706C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748403.1:n.349+31098G=