Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1244758G>A , CM000673.2:g.1244758G>A | GRCh38 |
| NC_000011.9:g.1265988G>A , CM000673.1:g.1265988G>A | GRCh37 |
| NC_000011.8:g.1222564G>A | NCBI36 |
| NG_031880.1:g.26694G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002458.3:c.7878G>A (MUC5B) MANE Select | NP_002449.2:p.Thr2626= |
| ENST00000529681.5:c.7878G>A (MUC5B) MANE Select | ENSP00000436812.1:p.Thr2626= |
| NM_002458.2:c.7878G>A (MUC5B) | NP_002449.2:p.Thr2626= |
| NR_157183.1:n.57-2120C>T (MUC5B-AS1) |