Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.65964482G= , CM000674.2:g.65964482G= | GRCh38 |
| NC_000012.11:g.66358262G= , CM000674.1:g.66358262G= | GRCh37 |
| NC_000012.10:g.64644529G= | NCBI36 |
| NG_016296.1:g.145023G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000403681.7:c.*1190G= MANE Select | ENSP00000384026.2:n.*1190G= | |
| ENST00000403681.6:c.*1190G= | ENSP00000384026.2:n.*1190G= | |
| NM_003483.4:c.*1190G= | NP_003474.1:n.*1190G= | |
| NM_003483.6:c.*1190G= MANE Select | NP_003474.1:n.*1190G= |