Canonical Allele Identifier: CA2645390667
Gene: MMACHC HGNC NCBI

Linked Data

gnomAD v4: 1-45500217-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500217C>T , CM000663.2:g.45500217C>T GRCh38
NC_000001.10:g.45965889C>T , CM000663.1:g.45965889C>T GRCh37
NC_000001.9:g.45738476C>T NCBI36
NG_013378.1:g.5034C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.8:c.-116C>T ENSP00000383840.4:n.-116C>T
NM_015506.2:c.-116C>T NP_056321.2:n.-116C>T
NM_001330540.1:c.-338C>T NP_001317469.1:n.-338C>T