Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127854355T= , CM000671.2:g.127854355T= | GRCh38 |
| NC_000009.11:g.130616634T= , CM000671.1:g.130616634T= | GRCh37 |
| NC_000009.10:g.129656455T= | NCBI36 |
| NG_009551.1:g.5414A= , LRG_589:g.5414A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001114753.3:c.1A= MANE Select | NP_001108225.1:p.Met1= |
| ENST00000373203.9:c.1A= MANE Select | ENSP00000362299.4:p.Met1= |
| NM_000118.3:c.1A= , LRG_589t1:c.1A= | NP_000109.1:p.Met1= |
| NM_001114753.2:c.1A= , LRG_589t2:c.1A= | NP_001108225.1:p.Met1= |
| ENST00000344849.4:c.1A= | ENSP00000341917.3:p.Met1= |
| ENST00000373203.8:c.1A= | ENSP00000362299.4:p.Met1= |