Canonical Allele Identifier: CA2516413066

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79114755C>T , CM000667.2:g.79114755C>T GRCh38
NC_000005.9:g.78410578C>T , CM000667.1:g.78410578C>T GRCh37
NC_000005.8:g.78446334C>T NCBI36
NG_029156.1:g.7975C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274353.10:c.34-1012C>T (BHMT) MANE Select ENSP00000274353.5:n.34-1012C>T
ENST00000274353.9:c.34-1012C>T (BHMT) ENSP00000274353.5:n.34-1012C>T
ENST00000520335.5:n.111-1012C>T (BHMT)
ENST00000520388.5:n.491+5586G>A (DMGDH)
ENST00000520703.1:n.111-1012C>T (BHMT)
ENST00000524080.1:c.34-1012C>T (BHMT) ENSP00000428240.1:n.34-1012C>T
NM_001713.2:c.34-1012C>T (BHMT) NP_001704.2:n.34-1012C>T
NM_001713.3:c.34-1012C>T (BHMT) MANE Select NP_001704.2:n.34-1012C>T