Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.80099829G= , CM000679.2:g.80099829G= | GRCh38 |
| NC_000017.10:g.78073628G= , CM000679.1:g.78073628G= | GRCh37 |
| NC_000017.9:g.75688223G= | NCBI36 |
| NG_009822.1:g.3274G= , LRG_673:g.3274G= | |
| NG_029761.1:g.68198G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000397545.9:c.*54G= MANE Select | ENSP00000380679.4:n.*54G= | |
| ENST00000397545.8:c.*54G= | ENSP00000380679.4:n.*54G= | |
| ENST00000574799.5:n.3020G= | ||
| NM_017950.3:c.*54G= | NP_060420.2:n.*54G= | |
| XM_011524963.1:c.*54G= | XP_011523265.1:n.*54G= | |
| XM_011524964.1:c.*54G= | XP_011523266.1:n.*54G= | |
| XM_011524963.3:c.*54G= | XP_011523265.1:n.*54G= | |
| XM_011524964.3:c.*54G= | XP_011523266.1:n.*54G= | |
| XM_024450821.1:c.*54G= | XP_024306589.1:n.*54G= | |
| XR_934495.2:n.3601G= | ||
| NM_017950.4:c.*54G= MANE Select | NP_060420.2:n.*54G= |