Canonical Allele Identifier: CA1608913986
Gene:

Linked Data

dbSNP Id: rs1759195251

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169772G>A , CM000668.2:g.8169772G>A GRCh38
NC_000006.11:g.8170005G>A , CM000668.1:g.8170005G>A GRCh37
NC_000006.10:g.8115004G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11512G>A
XR_926441.1:n.189+1852G>A
XR_926442.1:n.82+11512G>A
XR_926443.1:n.82+11512G>A
XR_001743950.1:n.179+1852G>A
XR_926440.2:n.74+11512G>A
XR_926441.2:n.179+1852G>A
XR_926443.2:n.83+11512G>A