Canonical Allele Identifier: CA2674379001

Linked Data

gnomAD v4: 5-79120601-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79120601T>A , CM000667.2:g.79120601T>A GRCh38
NC_000005.9:g.78416424T>A , CM000667.1:g.78416424T>A GRCh37
NC_000005.8:g.78452180T>A NCBI36
NG_029156.1:g.13821T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000274353.10:c.477+60T>A (BHMT) MANE Select ENSP00000274353.5:n.477+60T>A
ENST00000274353.9:c.477+60T>A (BHMT) ENSP00000274353.5:n.477+60T>A
ENST00000518707.1:n.279-148A>T (DMGDH)
ENST00000520388.5:n.379-148A>T (DMGDH)
ENST00000523508.1:n.190+60T>A (BHMT)
ENST00000524080.1:c.166+4702T>A (BHMT) ENSP00000428240.1:n.166+4702T>A
NM_001713.2:c.477+60T>A (BHMT) NP_001704.2:n.477+60T>A
NM_001713.3:c.477+60T>A (BHMT) MANE Select NP_001704.2:n.477+60T>A