Canonical Allele Identifier: CA2473780122
Gene: MMACHC HGNC NCBI

Linked Data

dbSNP Id: rs1643511204
gnomAD v4: 1-45500204-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500204T>A , CM000663.2:g.45500204T>A GRCh38
NC_000001.10:g.45965876T>A , CM000663.1:g.45965876T>A GRCh37
NC_000001.9:g.45738463T>A NCBI36
NG_013378.1:g.5021T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.8:c.-129T>A ENSP00000383840.4:n.-129T>A
NM_015506.2:c.-129T>A NP_056321.2:n.-129T>A
NM_001330540.1:c.-351T>A NP_001317469.1:n.-351T>A
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