Canonical Allele Identifier: CA1608914056
Gene:

Linked Data

dbSNP Id: rs1759196385

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169830A>G , CM000668.2:g.8169830A>G GRCh38
NC_000006.11:g.8170063A>G , CM000668.1:g.8170063A>G GRCh37
NC_000006.10:g.8115062A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11570A>G
XR_926441.1:n.189+1910A>G
XR_926442.1:n.82+11570A>G
XR_926443.1:n.82+11570A>G
XR_001743950.1:n.179+1910A>G
XR_926440.2:n.74+11570A>G
XR_926441.2:n.179+1910A>G
XR_926443.2:n.83+11570A>G