Canonical Allele Identifier: CA2136398913
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50856996T= , CM000676.2:g.50856996T= GRCh38
NC_000014.8:g.51323714T= , CM000676.1:g.51323714T= GRCh37
NC_000014.7:g.50393464T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943848.1:n.282+1102A=
XR_943848.2:n.643+1102A=