Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.79120533A= , CM000667.2:g.79120533A= | GRCh38 |
| NC_000005.9:g.78416356A= , CM000667.1:g.78416356A= | GRCh37 |
| NC_000005.8:g.78452112A= | NCBI36 |
| NG_029156.1:g.13753A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274353.10:c.469A= (BHMT) MANE Select | ENSP00000274353.5:p.Ile157= | |
| ENST00000274353.9:c.469A= (BHMT) | ENSP00000274353.5:p.Ile157= | |
| ENST00000518707.1:n.279-80T= (DMGDH) | ||
| ENST00000520388.5:n.379-80T= (DMGDH) | ||
| ENST00000523508.1:n.182A= (BHMT) | ||
| ENST00000524080.1:c.166+4634A= (BHMT) | ENSP00000428240.1:n.166+4634A= | |
| NM_001713.2:c.469A= (BHMT) | NP_001704.2:p.Ile157= | |
| NM_001713.3:c.469A= (BHMT) MANE Select | NP_001704.2:p.Ile157= |