Canonical Allele Identifier: CA827789
Gene: MMACHC HGNC NCBI

Linked Data

dbSNP Id: rs777345540
gnomAD v2: 1-45974595-G-A
gnomAD v4: 1-45508923-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508923G>A , CM000663.2:g.45508923G>A GRCh38
NC_000001.10:g.45974595G>A , CM000663.1:g.45974595G>A GRCh37
NC_000001.9:g.45747182G>A NCBI36
NG_013378.1:g.13740G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.557G>A MANE Select ENSP00000383840.4:p.Arg186Lys
ENST00000401061.8:c.557G>A ENSP00000383840.4:p.Arg186Lys
ENST00000616135.1:c.386G>A ENSP00000478859.1:p.Arg129Lys
NM_015506.2:c.557G>A NP_056321.2:p.Arg186Lys
XM_005270724.3:c.362G>A XP_005270781.1:p.Arg121Lys
XM_011541204.1:c.386G>A XP_011539506.1:p.Arg129Lys
NM_001330540.1:c.386G>A NP_001317469.1:p.Arg129Lys
XM_005270724.5:c.362G>A XP_005270781.1:p.Arg121Lys
NM_015506.3:c.557G>A MANE Select NP_056321.2:p.Arg186Lys
NM_001330540.2:c.386G>A NP_001317469.1:p.Arg129Lys