Canonical Allele Identifier: CA360201978
Gene: BHMT HGNC NCBI
DMGDH HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.78416239G>C (hg19) chr5:g.79120416G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79120416G>C , CM000667.2:g.79120416G>C GRCh38
NC_000005.9:g.78416239G>C , CM000667.1:g.78416239G>C GRCh37
NC_000005.8:g.78451995G>C NCBI36
NG_029156.1:g.13636G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000274353.10:c.352G>C (BHMT) MANE Select ENSP00000274353.5:p.Val118Leu
ENST00000274353.9:c.352G>C (BHMT) ENSP00000274353.5:p.Val118Leu
ENST00000518707.1:n.316C>G (DMGDH)
ENST00000520388.5:n.416C>G (DMGDH)
ENST00000523508.1:n.65G>C (BHMT)
ENST00000524080.1:c.166+4517G>C (BHMT) ENSP00000428240.1:n.166+4517G>C
NM_001713.2:c.352G>C (BHMT) NP_001704.2:p.Val118Leu
NM_001713.3:c.352G>C (BHMT) MANE Select NP_001704.2:p.Val118Leu
Search 100 bp 5'
Search 100 bp 3'