Canonical Allele Identifier: CA2740717966
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169771T>C , CM000668.2:g.8169771T>C GRCh38
NC_000006.11:g.8170004T>C , CM000668.1:g.8170004T>C GRCh37
NC_000006.10:g.8115003T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11511T>C
XR_926441.1:n.189+1851T>C
XR_926442.1:n.82+11511T>C
XR_926443.1:n.82+11511T>C
XR_001743950.1:n.179+1851T>C
XR_926440.2:n.74+11511T>C
XR_926441.2:n.179+1851T>C
XR_926443.2:n.83+11511T>C