Canonical Allele Identifier: CA417704571
Gene: MMACHC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.45973075G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45507403G>T , CM000663.2:g.45507403G>T GRCh38
NC_000001.10:g.45973075G>T , CM000663.1:g.45973075G>T GRCh37
NC_000001.9:g.45745662G>T NCBI36
NG_013378.1:g.12220G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.129G>T MANE Select ENSP00000383840.4:p.Leu43=
ENST00000401061.8:c.129G>T ENSP00000383840.4:p.Leu43=
ENST00000616135.1:c.-43G>T ENSP00000478859.1:n.-43G>T
NM_015506.2:c.129G>T NP_056321.2:p.Leu43=
XM_005270724.3:c.82-809G>T XP_005270781.1:n.82-809G>T
XM_011541204.1:c.-43G>T XP_011539506.1:n.-43G>T
NM_001330540.1:c.-43G>T NP_001317469.1:n.-43G>T
XM_005270724.5:c.82-809G>T XP_005270781.1:n.82-809G>T
NM_015506.3:c.129G>T MANE Select NP_056321.2:p.Leu43=
NM_001330540.2:c.-43G>T NP_001317469.1:n.-43G>T