Canonical Allele Identifier: CA417705505
Gene: MMACHC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.45973938C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508266C>A , CM000663.2:g.45508266C>A GRCh38
NC_000001.10:g.45973938C>A , CM000663.1:g.45973938C>A GRCh37
NC_000001.9:g.45746525C>A NCBI36
NG_013378.1:g.13083C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.331C>A MANE Select ENSP00000383840.4:p.Arg111=
ENST00000401061.8:c.331C>A ENSP00000383840.4:p.Arg111=
ENST00000616135.1:c.160C>A ENSP00000478859.1:p.Arg54=
NM_015506.2:c.331C>A NP_056321.2:p.Arg111=
XM_005270724.3:c.136C>A XP_005270781.1:p.Arg46=
XM_011541204.1:c.160C>A XP_011539506.1:p.Arg54=
NM_001330540.1:c.160C>A NP_001317469.1:p.Arg54=
XM_005270724.5:c.136C>A XP_005270781.1:p.Arg46=
NM_015506.3:c.331C>A MANE Select NP_056321.2:p.Arg111=
NM_001330540.2:c.160C>A NP_001317469.1:p.Arg54=