Canonical Allele Identifier: CA1596629084
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162656516T= , CM000667.2:g.162656516T= GRCh38
NC_000005.9:g.162083522T= , CM000667.1:g.162083522T= GRCh37
NC_000005.8:g.162016100T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742958.1:n.418+3586A=