Canonical Allele Identifier: CA340128275
Gene: MMACHC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500338G>T , CM000663.2:g.45500338G>T GRCh38
NC_000001.10:g.45966010G>T , CM000663.1:g.45966010G>T GRCh37
NC_000001.9:g.45738597G>T NCBI36
NG_013378.1:g.5155G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.6G>T MANE Select ENSP00000383840.4:p.Glu2Asp
ENST00000401061.8:c.6G>T ENSP00000383840.4:p.Glu2Asp
NM_015506.2:c.6G>T NP_056321.2:p.Glu2Asp
XM_005270724.3:c.6G>T XP_005270781.1:p.Glu2Asp
XM_011541204.1:c.-217G>T XP_011539506.1:n.-217G>T
NM_001330540.1:c.-217G>T NP_001317469.1:n.-217G>T
XM_005270724.5:c.6G>T XP_005270781.1:p.Glu2Asp
NM_015506.3:c.6G>T MANE Select NP_056321.2:p.Glu2Asp
NM_001330540.2:c.-217G>T NP_001317469.1:n.-217G>T