Canonical Allele Identifier: CA2298481223
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477650A= , CM000680.2:g.41477650A= GRCh38
NC_000018.9:g.39057614A= , CM000680.1:g.39057614A= GRCh37
NC_000018.8:g.37311612A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935409.1:n.86-26484A=