Canonical Allele Identifier: CA1596629175
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162656596T= , CM000667.2:g.162656596T= GRCh38
NC_000005.9:g.162083602T= , CM000667.1:g.162083602T= GRCh37
NC_000005.8:g.162016180T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742958.1:n.418+3506A=