Canonical Allele Identifier: CA827668
Gene: MMACHC HGNC NCBI

Linked Data

dbSNP Id: rs760657190
gnomAD v2: 1-45973171-G-A
gnomAD v3: 1-45507499-G-A
gnomAD v4: 1-45507499-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45507499G>A , CM000663.2:g.45507499G>A GRCh38
NC_000001.10:g.45973171G>A , CM000663.1:g.45973171G>A GRCh37
NC_000001.9:g.45745758G>A NCBI36
NG_013378.1:g.12316G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.225G>A MANE Select ENSP00000383840.4:p.Leu75=
ENST00000401061.8:c.225G>A ENSP00000383840.4:p.Leu75=
ENST00000616135.1:c.54G>A ENSP00000478859.1:p.Leu18=
NM_015506.2:c.225G>A NP_056321.2:p.Leu75=
XM_005270724.3:c.82-713G>A XP_005270781.1:n.82-713G>A
XM_011541204.1:c.54G>A XP_011539506.1:p.Leu18=
NM_001330540.1:c.54G>A NP_001317469.1:p.Leu18=
XM_005270724.5:c.82-713G>A XP_005270781.1:n.82-713G>A
NM_015506.3:c.225G>A MANE Select NP_056321.2:p.Leu75=
NM_001330540.2:c.54G>A NP_001317469.1:p.Leu18=