Canonical Allele Identifier: CA1146466312
Gene: MMACHC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500239A= , CM000663.2:g.45500239A= GRCh38
NC_000001.10:g.45965911A= , CM000663.1:g.45965911A= GRCh37
NC_000001.9:g.45738498A= NCBI36
NG_013378.1:g.5056A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.8:c.-94A= ENSP00000383840.4:n.-94A=
NM_015506.2:c.-94A= NP_056321.2:n.-94A=
NM_001330540.1:c.-316A= NP_001317469.1:n.-316A=
XM_005270724.5:c.-94A= XP_005270781.1:n.-94A=