Canonical Allele Identifier: CA340128258
Gene: MMACHC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500335G>C , CM000663.2:g.45500335G>C GRCh38
NC_000001.10:g.45966007G>C , CM000663.1:g.45966007G>C GRCh37
NC_000001.9:g.45738594G>C NCBI36
NG_013378.1:g.5152G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.3G>C MANE Select ENSP00000383840.4:p.Met1Ile
ENST00000401061.8:c.3G>C ENSP00000383840.4:p.Met1Ile
NM_015506.2:c.3G>C NP_056321.2:p.Met1Ile
XM_005270724.3:c.3G>C XP_005270781.1:p.Met1Ile
XM_011541204.1:c.-220G>C XP_011539506.1:n.-220G>C
NM_001330540.1:c.-220G>C NP_001317469.1:n.-220G>C
XM_005270724.5:c.3G>C XP_005270781.1:p.Met1Ile
NM_015506.3:c.3G>C MANE Select NP_056321.2:p.Met1Ile
NM_001330540.2:c.-220G>C NP_001317469.1:n.-220G>C