Canonical Allele Identifier: CA417704566
Gene: MMACHC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.45973069A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45507397A>T , CM000663.2:g.45507397A>T GRCh38
NC_000001.10:g.45973069A>T , CM000663.1:g.45973069A>T GRCh37
NC_000001.9:g.45745656A>T NCBI36
NG_013378.1:g.12214A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.123A>T MANE Select ENSP00000383840.4:p.Leu41=
ENST00000401061.8:c.123A>T ENSP00000383840.4:p.Leu41=
ENST00000616135.1:c.-49A>T ENSP00000478859.1:n.-49A>T
NM_015506.2:c.123A>T NP_056321.2:p.Leu41=
XM_005270724.3:c.82-815A>T XP_005270781.1:n.82-815A>T
XM_011541204.1:c.-49A>T XP_011539506.1:n.-49A>T
NM_001330540.1:c.-49A>T NP_001317469.1:n.-49A>T
XM_005270724.5:c.82-815A>T XP_005270781.1:n.82-815A>T
NM_015506.3:c.123A>T MANE Select NP_056321.2:p.Leu41=
NM_001330540.2:c.-49A>T NP_001317469.1:n.-49A>T