Canonical Allele Identifier: CA1557735479

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79120408A= , CM000667.2:g.79120408A= GRCh38
NC_000005.9:g.78416231A= , CM000667.1:g.78416231A= GRCh37
NC_000005.8:g.78451987A= NCBI36
NG_029156.1:g.13628A=

Transcript Alleles

HGVS Amino-acid change
ENST00000274353.10:c.344A= (BHMT) MANE Select ENSP00000274353.5:p.Asp115=
ENST00000274353.9:c.344A= (BHMT) ENSP00000274353.5:p.Asp115=
ENST00000518707.1:n.324T= (DMGDH)
ENST00000520388.5:n.424T= (DMGDH)
ENST00000523508.1:n.57A= (BHMT)
ENST00000524080.1:c.166+4509A= (BHMT) ENSP00000428240.1:n.166+4509A=
NM_001713.2:c.344A= (BHMT) NP_001704.2:p.Asp115=
NM_001713.3:c.344A= (BHMT) MANE Select NP_001704.2:p.Asp115=