Canonical Allele Identifier: CA417881453
Gene: MMACHC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.45974608C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508936C>A , CM000663.2:g.45508936C>A GRCh38
NC_000001.10:g.45974608C>A , CM000663.1:g.45974608C>A GRCh37
NC_000001.9:g.45747195C>A NCBI36
NG_013378.1:g.13753C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.9:c.570C>A MANE Select ENSP00000383840.4:p.Ile190=
ENST00000401061.8:c.570C>A ENSP00000383840.4:p.Ile190=
ENST00000616135.1:c.399C>A ENSP00000478859.1:p.Ile133=
NM_015506.2:c.570C>A NP_056321.2:p.Ile190=
XM_005270724.3:c.375C>A XP_005270781.1:p.Ile125=
XM_011541204.1:c.399C>A XP_011539506.1:p.Ile133=
NM_001330540.1:c.399C>A NP_001317469.1:p.Ile133=
XM_005270724.5:c.375C>A XP_005270781.1:p.Ile125=
NM_015506.3:c.570C>A MANE Select NP_056321.2:p.Ile190=
NM_001330540.2:c.399C>A NP_001317469.1:p.Ile133=