Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.79118514T= , CM000667.2:g.79118514T= | GRCh38 |
| NC_000005.9:g.78414337T= , CM000667.1:g.78414337T= | GRCh37 |
| NC_000005.8:g.78450093T= | NCBI36 |
| NG_029156.1:g.11734T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001713.3:c.167-745T= (BHMT) MANE Select | NP_001704.2:n.167-745T= |
| ENST00000274353.10:c.167-745T= (BHMT) MANE Select | ENSP00000274353.5:n.167-745T= |
| NM_001713.2:c.167-745T= (BHMT) | NP_001704.2:n.167-745T= |
| ENST00000274353.9:c.167-745T= (BHMT) | ENSP00000274353.5:n.167-745T= |
| ENST00000520388.5:n.491+1827A= (DMGDH) | |
| ENST00000520703.1:n.244-745T= (BHMT) | |
| ENST00000524080.1:c.166+2615T= (BHMT) | ENSP00000428240.1:n.166+2615T= |