Canonical Allele Identifier: CA2298481301
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477807G= , CM000680.2:g.41477807G= GRCh38
NC_000018.9:g.39057771G= , CM000680.1:g.39057771G= GRCh37
NC_000018.8:g.37311769G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935409.1:n.86-26327G=