Canonical Allele Identifier: CA340128281
Gene: MMACHC HGNC NCBI

Linked Data

gnomAD v4: 1-45500339-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500339C>G , CM000663.2:g.45500339C>G GRCh38
NC_000001.10:g.45966011C>G , CM000663.1:g.45966011C>G GRCh37
NC_000001.9:g.45738598C>G NCBI36
NG_013378.1:g.5156C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.7C>G MANE Select ENSP00000383840.4:p.Pro3Ala
ENST00000401061.8:c.7C>G ENSP00000383840.4:p.Pro3Ala
NM_015506.2:c.7C>G NP_056321.2:p.Pro3Ala
XM_005270724.3:c.7C>G XP_005270781.1:p.Pro3Ala
XM_011541204.1:c.-216C>G XP_011539506.1:n.-216C>G
NM_001330540.1:c.-216C>G NP_001317469.1:n.-216C>G
XM_005270724.5:c.7C>G XP_005270781.1:p.Pro3Ala
NM_015506.3:c.7C>G MANE Select NP_056321.2:p.Pro3Ala
NM_001330540.2:c.-216C>G NP_001317469.1:n.-216C>G