Canonical Allele Identifier: CA1146358567
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500280C= , CM000663.2:g.45500280C= GRCh38
NC_000001.10:g.45965952C= , CM000663.1:g.45965952C= GRCh37
NC_000001.9:g.45738539C= NCBI36
NG_013378.1:g.5097C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.8:c.-53C= ENSP00000383840.4:n.-53C=
NM_015506.2:c.-53C= NP_056321.2:n.-53C=
NM_001330540.1:c.-275C= NP_001317469.1:n.-275C=
XM_005270724.5:c.-53C= XP_005270781.1:n.-53C=