Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240875180G= , CM000664.2:g.240875180G= | GRCh38 |
| NC_000002.11:g.241814597G= , CM000664.1:g.241814597G= | GRCh37 |
| NC_000002.10:g.241463270G= | NCBI36 |
| NG_008005.1:g.11436G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.752G= MANE Select | ENSP00000302620.3:p.Trp251= | |
| ENST00000307503.3:c.752G= | ENSP00000302620.3:p.Trp251= | |
| ENST00000476698.1:n.404G= | ||
| NM_000030.2:c.752G= | NP_000021.1:p.Trp251= | |
| NM_000030.3:c.752G= MANE Select | NP_000021.1:p.Trp251= |