Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45500333A= , CM000663.2:g.45500333A= | GRCh38 |
| NC_000001.10:g.45966005A= , CM000663.1:g.45966005A= | GRCh37 |
| NC_000001.9:g.45738592A= | NCBI36 |
| NG_013378.1:g.5150A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_015506.3:c.1A= MANE Select | NP_056321.2:p.Met1= |
| ENST00000401061.9:c.1A= MANE Select | ENSP00000383840.4:p.Met1= |
| NM_001330540.1:c.-222A= | NP_001317469.1:n.-222A= |
| NM_001330540.2:c.-222A= | NP_001317469.1:n.-222A= |
| NM_015506.2:c.1A= | NP_056321.2:p.Met1= |
| ENST00000401061.8:c.1A= | ENSP00000383840.4:p.Met1= |
| XM_005270724.3:c.1A= | XP_005270781.1:p.Met1= |
| XM_005270724.5:c.1A= | XP_005270781.1:p.Met1= |
| XM_011541204.1:c.-222A= | XP_011539506.1:n.-222A= |