Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1248397C>T , CM000673.2:g.1248397C>T | GRCh38 |
| NC_000011.9:g.1269627C>T , CM000673.1:g.1269627C>T | GRCh37 |
| NC_000011.8:g.1226203C>T | NCBI36 |
| NG_031880.1:g.30333C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000529681.5:c.11517C>T (MUC5B) MANE Select | ENSP00000436812.1:p.Thr3839= | |
| NM_002458.2:c.11517C>T (MUC5B) | NP_002449.2:p.Thr3839= | |
| NR_157183.1:n.56+1224G>A (MUC5B-AS1) | ||
| NM_002458.3:c.11517C>T (MUC5B) MANE Select | NP_002449.2:p.Thr3839= |