HGVS | Genome Assembly |
---|---|
NC_000005.10:g.79120505C>G , CM000667.2:g.79120505C>G | GRCh38 |
NC_000005.9:g.78416328C>G , CM000667.1:g.78416328C>G | GRCh37 |
NC_000005.8:g.78452084C>G | NCBI36 |
NG_029156.1:g.13725C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000274353.10:c.441C>G (BHMT) MANE Select | ENSP00000274353.5:p.Val147= | |
ENST00000274353.9:c.441C>G (BHMT) | ENSP00000274353.5:p.Val147= | |
ENST00000518707.1:n.279-52G>C (DMGDH) | ||
ENST00000520388.5:n.379-52G>C (DMGDH) | ||
ENST00000523508.1:n.154C>G (BHMT) | ||
ENST00000524080.1:c.166+4606C>G (BHMT) | ENSP00000428240.1:n.166+4606C>G | |
NM_001713.2:c.441C>G (BHMT) | NP_001704.2:p.Val147= | |
NM_001713.3:c.441C>G (BHMT) MANE Select | NP_001704.2:p.Val147= |