Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5248393G= , CM000673.2:g.5248393G= | GRCh38 |
| NC_000011.9:g.5269623G= , CM000673.1:g.5269623G= | GRCh37 |
| NC_000011.8:g.5226199G= | NCBI36 |
| NG_000007.3:g.49223C= | |
| NG_063112.2:g.265C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000559.3:c.410C= (HBG1) MANE Select | NP_000550.2:p.Ala137= |
| ENST00000330597.5:c.410C= (HBG1) MANE Select | ENSP00000327431.4:p.Ala137= |
| NM_000559.2:c.410C= (HBG1) | NP_000550.2:p.Ala137= |
| ENST00000330597.3:c.410C= (HBG1) | ENSP00000327431.3:p.Ala137= |
| ENST00000620888.4:c.410C= (HBG2) | ENSP00000479637.1:p.Ala137= |
| ENST00000642908.1:c.410C= | ENSP00000495346.1:p.Ala137= |
| ENST00000647543.1:c.473C= | ENSP00000496470.1:p.Ala158= |
| ENST00000648735.1:n.1341C= (HBG1) |