Canonical Allele Identifier: CA12118097

Linked Data

dbSNP Id: rs10037045

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79126747A>T , CM000667.2:g.79126747A>T GRCh38
NC_000005.9:g.78422570A>T , CM000667.1:g.78422570A>T GRCh37
NC_000005.8:g.78458326A>T NCBI36
NG_029156.1:g.19967A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274353.10:c.808+519A>T (BHMT) MANE Select ENSP00000274353.5:n.808+519A>T
ENST00000274353.9:c.808+519A>T (BHMT) ENSP00000274353.5:n.808+519A>T
ENST00000518707.1:n.129-5395T>A (DMGDH)
ENST00000520388.5:n.229-5395T>A (DMGDH)
ENST00000521279.1:n.268+519A>T (BHMT)
ENST00000524080.1:c.349+519A>T (BHMT) ENSP00000428240.1:n.349+519A>T
NM_001713.2:c.808+519A>T (BHMT) NP_001704.2:n.808+519A>T
NM_001713.3:c.808+519A>T (BHMT) MANE Select NP_001704.2:n.808+519A>T