Canonical Allele Identifier: CA417705498
Gene: MMACHC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.45973928G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508256G>T , CM000663.2:g.45508256G>T GRCh38
NC_000001.10:g.45973928G>T , CM000663.1:g.45973928G>T GRCh37
NC_000001.9:g.45746515G>T NCBI36
NG_013378.1:g.13073G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.321G>T MANE Select ENSP00000383840.4:p.Val107=
ENST00000401061.8:c.321G>T ENSP00000383840.4:p.Val107=
ENST00000616135.1:c.150G>T ENSP00000478859.1:p.Val50=
NM_015506.2:c.321G>T NP_056321.2:p.Val107=
XM_005270724.3:c.126G>T XP_005270781.1:p.Val42=
XM_011541204.1:c.150G>T XP_011539506.1:p.Val50=
NM_001330540.1:c.150G>T NP_001317469.1:p.Val50=
XM_005270724.5:c.126G>T XP_005270781.1:p.Val42=
NM_015506.3:c.321G>T MANE Select NP_056321.2:p.Val107=
NM_001330540.2:c.150G>T NP_001317469.1:p.Val50=