Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.176717A= , CM000678.2:g.176717A= | GRCh38 |
| NC_000016.9:g.226716A= , CM000678.1:g.226716A= | GRCh37 |
| NC_000016.8:g.166716A= | NCBI36 |
| NG_000006.1:g.37580A= | |
| NG_059186.1:g.5067A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000558.5:c.1A= MANE Select | NP_000549.1:p.Met1= |
| ENST00000320868.9:c.1A= MANE Select | ENSP00000322421.5:p.Met1= |
| NM_000558.4:c.1A= | NP_000549.1:p.Met1= |
| ENST00000397797.1:c.-47A= | ENSP00000380899.1:n.-47A= |
| ENST00000472694.1:n.20A= |