Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5248418C= , CM000673.2:g.5248418C= | GRCh38 |
| NC_000011.9:g.5269648C= , CM000673.1:g.5269648C= | GRCh37 |
| NC_000011.8:g.5226224C= | NCBI36 |
| NG_000007.3:g.49198G= | |
| NG_063112.2:g.240G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000559.3:c.385G= (HBG1) MANE Select | NP_000550.2:p.Ala129= |
| ENST00000330597.5:c.385G= (HBG1) MANE Select | ENSP00000327431.4:p.Ala129= |
| NM_000559.2:c.385G= (HBG1) | NP_000550.2:p.Ala129= |
| ENST00000330597.3:c.385G= (HBG1) | ENSP00000327431.3:p.Ala129= |
| ENST00000620888.4:c.385G= (HBG2) | ENSP00000479637.1:p.Ala129= |
| ENST00000642908.1:c.385G= | ENSP00000495346.1:p.Ala129= |
| ENST00000647543.1:c.448G= | ENSP00000496470.1:p.Ala150= |
| ENST00000648735.1:n.1316G= (HBG1) |