Canonical Allele Identifier: CA417881451

Gene: MMACHC

Linked Data

• MyVariant Identifiers: chr1:g.45974605T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45508933T>G , CM000663.2:g.45508933T>G	GRCh38
NC_000001.10:g.45974605T>G , CM000663.1:g.45974605T>G	GRCh37
NC_000001.9:g.45747192T>G	NCBI36
NG_013378.1:g.13750T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.567T>G MANE Select	ENSP00000383840.4:p.Arg189=
ENST00000401061.8:c.567T>G	ENSP00000383840.4:p.Arg189=
ENST00000616135.1:c.396T>G	ENSP00000478859.1:p.Arg132=
NM_015506.2:c.567T>G	NP_056321.2:p.Arg189=
XM_005270724.3:c.372T>G	XP_005270781.1:p.Arg124=
XM_011541204.1:c.396T>G	XP_011539506.1:p.Arg132=
NM_001330540.1:c.396T>G	NP_001317469.1:p.Arg132=
XM_005270724.5:c.372T>G	XP_005270781.1:p.Arg124=
NM_015506.3:c.567T>G MANE Select	NP_056321.2:p.Arg189=
NM_001330540.2:c.396T>G	NP_001317469.1:p.Arg132=