HGVS | Genome Assembly |
---|---|
NC_000005.10:g.79120659T>C , CM000667.2:g.79120659T>C | GRCh38 |
NC_000005.9:g.78416482T>C , CM000667.1:g.78416482T>C | GRCh37 |
NC_000005.8:g.78452238T>C | NCBI36 |
NG_029156.1:g.13879T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000274353.10:c.477+118T>C (BHMT) MANE Select | ENSP00000274353.5:n.477+118T>C | |
ENST00000274353.9:c.477+118T>C (BHMT) | ENSP00000274353.5:n.477+118T>C | |
ENST00000518707.1:n.279-206A>G (DMGDH) | ||
ENST00000520388.5:n.379-206A>G (DMGDH) | ||
ENST00000523508.1:n.190+118T>C (BHMT) | ||
ENST00000524080.1:c.166+4760T>C (BHMT) | ENSP00000428240.1:n.166+4760T>C | |
NM_001713.2:c.477+118T>C (BHMT) | NP_001704.2:n.477+118T>C | |
NM_001713.3:c.477+118T>C (BHMT) MANE Select | NP_001704.2:n.477+118T>C |