Canonical Allele Identifier: CA1728106719
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388449A= , CM000669.2:g.97388449A= GRCh38
NC_000007.13:g.97017761A= , CM000669.1:g.97017761A= GRCh37
NC_000007.12:g.96855697A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59802T=