Canonical Allele Identifier: CA340132502
Gene: MMACHC HGNC NCBI

Linked Data

ClinVar Variation Id: 1446343
ClinVar RCV Id: RCV001958489
dbSNP Id: rs2149323618

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508354G>A , CM000663.2:g.45508354G>A GRCh38
NC_000001.10:g.45974026G>A , CM000663.1:g.45974026G>A GRCh37
NC_000001.9:g.45746613G>A NCBI36
NG_013378.1:g.13171G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.419G>A MANE Select ENSP00000383840.4:p.Trp140Ter
ENST00000401061.8:c.419G>A ENSP00000383840.4:p.Trp140Ter
ENST00000616135.1:c.248G>A ENSP00000478859.1:p.Trp83Ter
NM_015506.2:c.419G>A NP_056321.2:p.Trp140Ter
XM_005270724.3:c.224G>A XP_005270781.1:p.Trp75Ter
XM_011541204.1:c.248G>A XP_011539506.1:p.Trp83Ter
NM_001330540.1:c.248G>A NP_001317469.1:p.Trp83Ter
XM_005270724.5:c.224G>A XP_005270781.1:p.Trp75Ter
NM_015506.3:c.419G>A MANE Select NP_056321.2:p.Trp140Ter
NM_001330540.2:c.248G>A NP_001317469.1:p.Trp83Ter