Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44286007A= , CM000683.2:g.44286007A= | GRCh38 |
| NC_000021.8:g.45705890A= , CM000683.1:g.45705890A= | GRCh37 |
| NC_000021.7:g.44530318A= | NCBI36 |
| NG_009556.1:g.5128A= , LRG_18:g.5128A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000383.4:c.1A= MANE Select | NP_000374.1:p.Met1= |
| ENST00000291582.6:c.1A= MANE Select | ENSP00000291582.5:p.Met1= |
| NM_000383.3:c.1A= | NP_000374.1:p.Met1= |
| ENST00000291582.5:c.1A= | ENSP00000291582.5:p.Met1= |
| ENST00000527919.5:n.162A= | |
| ENST00000530812.5:n.170A= | |
| XM_011529551.1:c.1A= | XP_011527853.1:p.Met1= |