Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.79114732T= , CM000667.2:g.79114732T= | GRCh38 |
| NC_000005.9:g.78410555T= , CM000667.1:g.78410555T= | GRCh37 |
| NC_000005.8:g.78446311T= | NCBI36 |
| NG_029156.1:g.7952T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274353.10:c.34-1035T= (BHMT) MANE Select | ENSP00000274353.5:n.34-1035T= | |
| ENST00000274353.9:c.34-1035T= (BHMT) | ENSP00000274353.5:n.34-1035T= | |
| ENST00000520335.5:n.111-1035T= (BHMT) | ||
| ENST00000520388.5:n.491+5609A= (DMGDH) | ||
| ENST00000520703.1:n.111-1035T= (BHMT) | ||
| ENST00000524080.1:c.34-1035T= (BHMT) | ENSP00000428240.1:n.34-1035T= | |
| NM_001713.2:c.34-1035T= (BHMT) | NP_001704.2:n.34-1035T= | |
| NM_001713.3:c.34-1035T= (BHMT) MANE Select | NP_001704.2:n.34-1035T= |