Canonical Allele Identifier: CA1557732029

Gene: BHMT DMGDH

Linked Data

• dbSNP Id: rs1756361175

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.79114813T>C , CM000667.2:g.79114813T>C	GRCh38
NC_000005.9:g.78410636T>C , CM000667.1:g.78410636T>C	GRCh37
NC_000005.8:g.78446392T>C	NCBI36
NG_029156.1:g.8033T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000274353.10:c.34-954T>C (BHMT) MANE Select	ENSP00000274353.5:n.34-954T>C
ENST00000274353.9:c.34-954T>C (BHMT)	ENSP00000274353.5:n.34-954T>C
ENST00000520335.5:n.111-954T>C (BHMT)
ENST00000520388.5:n.491+5528A>G (DMGDH)
ENST00000520703.1:n.111-954T>C (BHMT)
ENST00000524080.1:c.34-954T>C (BHMT)	ENSP00000428240.1:n.34-954T>C
NM_001713.2:c.34-954T>C (BHMT)	NP_001704.2:n.34-954T>C
NM_001713.3:c.34-954T>C (BHMT) MANE Select	NP_001704.2:n.34-954T>C