Canonical Allele Identifier: CA1728106723
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388458G= , CM000669.2:g.97388458G= GRCh38
NC_000007.13:g.97017770G= , CM000669.1:g.97017770G= GRCh37
NC_000007.12:g.96855706G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59811C=