Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.72888457A= , CM000664.2:g.72888457A= | GRCh38 |
| NC_000002.11:g.73115586A= , CM000664.1:g.73115586A= | GRCh37 |
| NC_000002.10:g.72969094A= | NCBI36 |
| NG_008234.1:g.6075A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003124.5:c.448A= MANE Select | NP_003115.1:p.Arg150= |
| ENST00000234454.6:c.448A= MANE Select | ENSP00000234454.5:p.Arg150= |
| NM_003124.4:c.448A= | NP_003115.1:p.Arg150= |
| ENST00000234454.5:c.448A= | ENSP00000234454.5:p.Arg150= |
| ENST00000498749.1:n.393A= |