Canonical Allele Identifier: CA2386490951
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33035869C= , CM000683.2:g.33035869C= GRCh38
NC_000021.8:g.34408177C= , CM000683.1:g.34408177C= GRCh37
NC_000021.7:g.33330047C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937672.1:n.89+242C=
XR_937672.3:n.289+242C=
XR_937673.1:n.172+40C=
XR_937673.2:n.120+40C=