Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1246095T>C , CM000673.2:g.1246095T>C | GRCh38 |
| NC_000011.9:g.1267325T>C , CM000673.1:g.1267325T>C | GRCh37 |
| NC_000011.8:g.1223901T>C | NCBI36 |
| NG_031880.1:g.28031T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002458.3:c.9215T>C (MUC5B) MANE Select | NP_002449.2:p.Phe3072Ser |
| ENST00000529681.5:c.9215T>C (MUC5B) MANE Select | ENSP00000436812.1:p.Phe3072Ser |
| NM_002458.2:c.9215T>C (MUC5B) | NP_002449.2:p.Phe3072Ser |
| NR_157183.1:n.57-3457A>G (MUC5B-AS1) |