Canonical Allele Identifier: CA134548300
Gene:

Linked Data

dbSNP Id: rs1003569981
gnomAD v2: 6-8170059-C-G
gnomAD v3: 6-8169826-C-G
gnomAD v4: 6-8169826-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169826C>G , CM000668.2:g.8169826C>G GRCh38
NC_000006.11:g.8170059C>G , CM000668.1:g.8170059C>G GRCh37
NC_000006.10:g.8115058C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11566C>G
XR_926441.1:n.189+1906C>G
XR_926442.1:n.82+11566C>G
XR_926443.1:n.82+11566C>G
XR_001743950.1:n.179+1906C>G
XR_926440.2:n.74+11566C>G
XR_926441.2:n.179+1906C>G
XR_926443.2:n.83+11566C>G