Linked Data
dbSNP Id:
rs1485077194
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29946132G>A , CM000668.2:g.29946132G>A | GRCh38 |
| NC_000006.11:g.29913909G>A , CM000668.1:g.29913909G>A | GRCh37 |
| NC_000006.10:g.30021888G>A | NCBI36 |
| NG_029217.2:g.8668G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706901.1:c.*677G>A | ENSP00000516612.1:n.*677G>A | |
| ENST00000706902.1:c.1093+851G>A | ENSP00000516613.1:n.1093+851G>A | |
| ENST00000706903.1:c.*124+553G>A | ENSP00000516614.1:n.*124+553G>A | |
| ENST00000706904.1:c.1093+851G>A | ENSP00000516615.1:n.1093+851G>A | |
| ENST00000706905.1:c.*677G>A | ENSP00000516616.1:n.*677G>A |