Canonical Allele Identifier: CA827664
Gene: MMACHC HGNC NCBI

Linked Data

dbSNP Id: rs1553162783
gnomAD v2: 1-45973164-G-A
gnomAD v4: 1-45507492-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45507492G>A , CM000663.2:g.45507492G>A GRCh38
NC_000001.10:g.45973164G>A , CM000663.1:g.45973164G>A GRCh37
NC_000001.9:g.45745751G>A NCBI36
NG_013378.1:g.12309G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.218G>A MANE Select ENSP00000383840.4:p.Arg73Gln
ENST00000401061.8:c.218G>A ENSP00000383840.4:p.Arg73Gln
ENST00000616135.1:c.47G>A ENSP00000478859.1:p.Arg16Gln
NM_015506.2:c.218G>A NP_056321.2:p.Arg73Gln
XM_005270724.3:c.82-720G>A XP_005270781.1:n.82-720G>A
XM_011541204.1:c.47G>A XP_011539506.1:p.Arg16Gln
NM_001330540.1:c.47G>A NP_001317469.1:p.Arg16Gln
XM_005270724.5:c.82-720G>A XP_005270781.1:n.82-720G>A
NM_015506.3:c.218G>A MANE Select NP_056321.2:p.Arg73Gln
NM_001330540.2:c.47G>A NP_001317469.1:p.Arg16Gln