Canonical Allele Identifier: CA1608913722
Gene:

Linked Data

dbSNP Id: rs1689078156

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169510C>G , CM000668.2:g.8169510C>G GRCh38
NC_000006.11:g.8169743C>G , CM000668.1:g.8169743C>G GRCh37
NC_000006.10:g.8114742C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11250C>G
XR_926441.1:n.189+1590C>G
XR_926442.1:n.82+11250C>G
XR_926443.1:n.82+11250C>G
XR_001743950.1:n.179+1590C>G
XR_926440.2:n.74+11250C>G
XR_926441.2:n.179+1590C>G
XR_926443.2:n.83+11250C>G