Linked Data
gnomAD v4:
5-79120636-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.79120636T>A , CM000667.2:g.79120636T>A | GRCh38 |
| NC_000005.9:g.78416459T>A , CM000667.1:g.78416459T>A | GRCh37 |
| NC_000005.8:g.78452215T>A | NCBI36 |
| NG_029156.1:g.13856T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274353.10:c.477+95T>A (BHMT) MANE Select | ENSP00000274353.5:n.477+95T>A | |
| ENST00000274353.9:c.477+95T>A (BHMT) | ENSP00000274353.5:n.477+95T>A | |
| ENST00000518707.1:n.279-183A>T (DMGDH) | ||
| ENST00000520388.5:n.379-183A>T (DMGDH) | ||
| ENST00000523508.1:n.190+95T>A (BHMT) | ||
| ENST00000524080.1:c.166+4737T>A (BHMT) | ENSP00000428240.1:n.166+4737T>A | |
| NM_001713.2:c.477+95T>A (BHMT) | NP_001704.2:n.477+95T>A | |
| NM_001713.3:c.477+95T>A (BHMT) MANE Select | NP_001704.2:n.477+95T>A |