Canonical Allele Identifier: CA360201963
Gene: BHMT HGNC NCBI
DMGDH HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.78416237T>C (hg19) chr5:g.79120414T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79120414T>C , CM000667.2:g.79120414T>C GRCh38
NC_000005.9:g.78416237T>C , CM000667.1:g.78416237T>C GRCh37
NC_000005.8:g.78451993T>C NCBI36
NG_029156.1:g.13634T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274353.10:c.350T>C (BHMT) MANE Select ENSP00000274353.5:p.Leu117Ser
ENST00000274353.9:c.350T>C (BHMT) ENSP00000274353.5:p.Leu117Ser
ENST00000518707.1:n.318A>G (DMGDH)
ENST00000520388.5:n.418A>G (DMGDH)
ENST00000523508.1:n.63T>C (BHMT)
ENST00000524080.1:c.166+4515T>C (BHMT) ENSP00000428240.1:n.166+4515T>C
NM_001713.2:c.350T>C (BHMT) NP_001704.2:p.Leu117Ser
NM_001713.3:c.350T>C (BHMT) MANE Select NP_001704.2:p.Leu117Ser
Search 100 bp 5'
Search 100 bp 3'