Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1245486T>C , CM000673.2:g.1245486T>C | GRCh38 |
| NC_000011.9:g.1266716T>C , CM000673.1:g.1266716T>C | GRCh37 |
| NC_000011.8:g.1223292T>C | NCBI36 |
| NG_031880.1:g.27422T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000529681.5:c.8606T>C (MUC5B) MANE Select | ENSP00000436812.1:p.Met2869Thr | |
| NM_002458.2:c.8606T>C (MUC5B) | NP_002449.2:p.Met2869Thr | |
| NR_157183.1:n.57-2848A>G (MUC5B-AS1) | ||
| NM_002458.3:c.8606T>C (MUC5B) MANE Select | NP_002449.2:p.Met2869Thr |