Canonical Allele Identifier: CA445104684

Linked Data

MyVariant Identifiers: chr5:g.78416229A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79120406A>G , CM000667.2:g.79120406A>G GRCh38
NC_000005.9:g.78416229A>G , CM000667.1:g.78416229A>G GRCh37
NC_000005.8:g.78451985A>G NCBI36
NG_029156.1:g.13626A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274353.10:c.342A>G (BHMT) MANE Select ENSP00000274353.5:p.Gly114=
ENST00000274353.9:c.342A>G (BHMT) ENSP00000274353.5:p.Gly114=
ENST00000518707.1:n.326T>C (DMGDH)
ENST00000520388.5:n.426T>C (DMGDH)
ENST00000523508.1:n.55A>G (BHMT)
ENST00000524080.1:c.166+4507A>G (BHMT) ENSP00000428240.1:n.166+4507A>G
NM_001713.2:c.342A>G (BHMT) NP_001704.2:p.Gly114=
NM_001713.3:c.342A>G (BHMT) MANE Select NP_001704.2:p.Gly114=