Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110155300C= , CM000675.2:g.110155300C= | GRCh38 |
| NC_000013.10:g.110807647C= , CM000675.1:g.110807647C= | GRCh37 |
| NC_000013.9:g.109605648C= | NCBI36 |
| NG_011544.2:g.156850G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001845.6:c.4738G= MANE Select | NP_001836.3:p.Gly1580= |
| ENST00000375820.10:c.4738G= MANE Select | ENSP00000364979.4:p.Gly1580= |
| NM_001845.5:c.4738G= | NP_001836.3:p.Gly1580= |
| ENST00000375820.8:c.4738G= | ENSP00000364979.4:p.Gly1580= |
| ENST00000649720.1:n.906G= | |
| ENST00000650424.1:c.894G= | |
| XM_011521048.1:c.4546G= | XP_011519350.1:p.Gly1516= |
| XM_011521048.2:c.4546G= | XP_011519350.1:p.Gly1516= |