Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.28767700G= , CM000676.2:g.28767700G= | GRCh38 |
| NC_000014.8:g.29236906G= , CM000676.1:g.29236906G= | GRCh37 |
| NC_000014.7:g.28306657G= | NCBI36 |
| NG_009367.1:g.5620G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000706482.1:c.421G= | ENSP00000516406.1:p.Gly141= | |
| ENST00000313071.7:c.421G= MANE Select | ENSP00000339004.3:p.Gly141= | |
| ENST00000313071.6:c.421G= | ENSP00000339004.3:p.Gly141= | |
| NM_005249.4:c.421G= | NP_005240.3:p.Gly141= | |
| NM_005249.5:c.421G= MANE Select | NP_005240.3:p.Gly141= |