Linked Data
dbSNP Id:
rs1771660023
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29946097C>A , CM000668.2:g.29946097C>A | GRCh38 |
| NC_000006.11:g.29913874C>A , CM000668.1:g.29913874C>A | GRCh37 |
| NC_000006.10:g.30021853C>A | NCBI36 |
| NG_029217.2:g.8633C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706901.1:c.*642C>A | ENSP00000516612.1:n.*642C>A | |
| ENST00000706902.1:c.1093+816C>A | ENSP00000516613.1:n.1093+816C>A | |
| ENST00000706903.1:c.*124+518C>A | ENSP00000516614.1:n.*124+518C>A | |
| ENST00000706904.1:c.1093+816C>A | ENSP00000516615.1:n.1093+816C>A | |
| ENST00000706905.1:c.*642C>A | ENSP00000516616.1:n.*642C>A |