Canonical Allele Identifier: CA736184960
Gene: MMACHC HGNC NCBI

Linked Data

dbSNP Id: rs1452290936
gnomAD v4: 1-45500276-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500276C>T , CM000663.2:g.45500276C>T GRCh38
NC_000001.10:g.45965948C>T , CM000663.1:g.45965948C>T GRCh37
NC_000001.9:g.45738535C>T NCBI36
NG_013378.1:g.5093C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.8:c.-57C>T ENSP00000383840.4:n.-57C>T
NM_015506.2:c.-57C>T NP_056321.2:n.-57C>T
NM_001330540.1:c.-279C>T NP_001317469.1:n.-279C>T
XM_005270724.5:c.-57C>T XP_005270781.1:n.-57C>T