Canonical Allele Identifier: CA565403894
Gene:

Linked Data

dbSNP Id: rs1035593959
gnomAD v2: 6-8170061-C-G
gnomAD v3: 6-8169828-C-G
gnomAD v4: 6-8169828-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169828C>G , CM000668.2:g.8169828C>G GRCh38
NC_000006.11:g.8170061C>G , CM000668.1:g.8170061C>G GRCh37
NC_000006.10:g.8115060C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11568C>G
XR_926441.1:n.189+1908C>G
XR_926442.1:n.82+11568C>G
XR_926443.1:n.82+11568C>G
XR_001743950.1:n.179+1908C>G
XR_926440.2:n.74+11568C>G
XR_926441.2:n.179+1908C>G
XR_926443.2:n.83+11568C>G