Canonical Allele Identifier: CA1557744808
Gene: BHMT HGNC NCBI
DMGDH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79126720C= , CM000667.2:g.79126720C= GRCh38
NC_000005.9:g.78422543C= , CM000667.1:g.78422543C= GRCh37
NC_000005.8:g.78458299C= NCBI36
NG_029156.1:g.19940C=

Transcript Alleles

HGVS Amino-acid change
ENST00000274353.10:c.808+492C= (BHMT) MANE Select ENSP00000274353.5:n.808+492C=
ENST00000274353.9:c.808+492C= (BHMT) ENSP00000274353.5:n.808+492C=
ENST00000518707.1:n.129-5368G= (DMGDH)
ENST00000520388.5:n.229-5368G= (DMGDH)
ENST00000521279.1:n.268+492C= (BHMT)
ENST00000524080.1:c.349+492C= (BHMT) ENSP00000428240.1:n.349+492C=
NM_001713.2:c.808+492C= (BHMT) NP_001704.2:n.808+492C=
NM_001713.3:c.808+492C= (BHMT) MANE Select NP_001704.2:n.808+492C=
Search 100 bp 5'
Search 100 bp 3'