Canonical Allele Identifier: CA2298481268
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477746G= , CM000680.2:g.41477746G= GRCh38
NC_000018.9:g.39057710G= , CM000680.1:g.39057710G= GRCh37
NC_000018.8:g.37311708G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935409.1:n.86-26388G=