Canonical Allele Identifier: CA417881432
Gene: MMACHC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.45974594A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508922A>C , CM000663.2:g.45508922A>C GRCh38
NC_000001.10:g.45974594A>C , CM000663.1:g.45974594A>C GRCh37
NC_000001.9:g.45747181A>C NCBI36
NG_013378.1:g.13739A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.556A>C MANE Select ENSP00000383840.4:p.Arg186=
ENST00000401061.8:c.556A>C ENSP00000383840.4:p.Arg186=
ENST00000616135.1:c.385A>C ENSP00000478859.1:p.Arg129=
NM_015506.2:c.556A>C NP_056321.2:p.Arg186=
XM_005270724.3:c.361A>C XP_005270781.1:p.Arg121=
XM_011541204.1:c.385A>C XP_011539506.1:p.Arg129=
NM_001330540.1:c.385A>C NP_001317469.1:p.Arg129=
XM_005270724.5:c.361A>C XP_005270781.1:p.Arg121=
NM_015506.3:c.556A>C MANE Select NP_056321.2:p.Arg186=
NM_001330540.2:c.385A>C NP_001317469.1:p.Arg129=