Canonical Allele Identifier:
CA2002397790
Gene:
Linked Data
dbSNP Id:
rs1591465626
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116072618A>C , CM000673.2:g.116072618A>C | GRCh38 |
| NC_000011.9:g.115943336A>C , CM000673.1:g.115943336A>C | GRCh37 |
| NC_000011.8:g.115448546A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_948055.1:n.192+396T>G | ||
| XR_948056.1:n.311-5413T>G | ||
| XR_948057.1:n.97+491T>G | ||
| XR_001748401.1:n.192+396T>G | ||
| XR_948055.2:n.192+396T>G | ||
| XR_948056.2:n.314-5413T>G | ||
| XR_948057.2:n.97+491T>G |