Canonical Allele Identifier: CA340133458
Gene: MMACHC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508928G>C , CM000663.2:g.45508928G>C GRCh38
NC_000001.10:g.45974600G>C , CM000663.1:g.45974600G>C GRCh37
NC_000001.9:g.45747187G>C NCBI36
NG_013378.1:g.13745G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.562G>C MANE Select ENSP00000383840.4:p.Asp188His
ENST00000401061.8:c.562G>C ENSP00000383840.4:p.Asp188His
ENST00000616135.1:c.391G>C ENSP00000478859.1:p.Asp131His
NM_015506.2:c.562G>C NP_056321.2:p.Asp188His
XM_005270724.3:c.367G>C XP_005270781.1:p.Asp123His
XM_011541204.1:c.391G>C XP_011539506.1:p.Asp131His
NM_001330540.1:c.391G>C NP_001317469.1:p.Asp131His
XM_005270724.5:c.367G>C XP_005270781.1:p.Asp123His
NM_015506.3:c.562G>C MANE Select NP_056321.2:p.Asp188His
NM_001330540.2:c.391G>C NP_001317469.1:p.Asp131His