Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.46739505G= , CM000673.2:g.46739505G= | GRCh38 |
| NC_000011.9:g.46761055G= , CM000673.1:g.46761055G= | GRCh37 |
| NC_000011.8:g.46717631G= | NCBI36 |
| NG_008953.1:g.25313G= , LRG_551:g.25313G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000506.5:c.*97G= MANE Select | NP_000497.1:n.*97G= |
| ENST00000311907.10:c.*97G= MANE Select | ENSP00000308541.5:n.*97G= |
| NM_000506.3:c.*97G= | NP_000497.1:n.*97G= |
| NM_000506.4:c.*97G= , LRG_551t1:c.*97G= | NP_000497.1:n.*97G= |
| NM_001311257.1:c.*97G= | NP_001298186.1:n.*97G= |
| NM_001311257.2:c.*97G= | NP_001298186.1:n.*97G= |
| ENST00000311907.9:c.*97G= | ENSP00000308541.5:n.*97G= |