Canonical Allele Identifier: CA340132193
Gene: MMACHC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508259C>A , CM000663.2:g.45508259C>A GRCh38
NC_000001.10:g.45973931C>A , CM000663.1:g.45973931C>A GRCh37
NC_000001.9:g.45746518C>A NCBI36
NG_013378.1:g.13076C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.324C>A MANE Select ENSP00000383840.4:p.His108Gln
ENST00000401061.8:c.324C>A ENSP00000383840.4:p.His108Gln
ENST00000616135.1:c.153C>A ENSP00000478859.1:p.His51Gln
NM_015506.2:c.324C>A NP_056321.2:p.His108Gln
XM_005270724.3:c.129C>A XP_005270781.1:p.His43Gln
XM_011541204.1:c.153C>A XP_011539506.1:p.His51Gln
NM_001330540.1:c.153C>A NP_001317469.1:p.His51Gln
XM_005270724.5:c.129C>A XP_005270781.1:p.His43Gln
NM_015506.3:c.324C>A MANE Select NP_056321.2:p.His108Gln
NM_001330540.2:c.153C>A NP_001317469.1:p.His51Gln