Canonical Allele Identifier: CA445104689

Linked Data

dbSNP Id: rs1580270854
gnomAD v4: 5-79120409-T-C
MyVariant Identifiers: chr5:g.78416232T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79120409T>C , CM000667.2:g.79120409T>C GRCh38
NC_000005.9:g.78416232T>C , CM000667.1:g.78416232T>C GRCh37
NC_000005.8:g.78451988T>C NCBI36
NG_029156.1:g.13629T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274353.10:c.345T>C (BHMT) MANE Select ENSP00000274353.5:p.Asp115=
ENST00000274353.9:c.345T>C (BHMT) ENSP00000274353.5:p.Asp115=
ENST00000518707.1:n.323A>G (DMGDH)
ENST00000520388.5:n.423A>G (DMGDH)
ENST00000523508.1:n.58T>C (BHMT)
ENST00000524080.1:c.166+4510T>C (BHMT) ENSP00000428240.1:n.166+4510T>C
NM_001713.2:c.345T>C (BHMT) NP_001704.2:p.Asp115=
NM_001713.3:c.345T>C (BHMT) MANE Select NP_001704.2:p.Asp115=