Canonical Allele Identifier: CA21825921
Gene: MMACHC HGNC NCBI

Linked Data

dbSNP Id: rs902026116

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500347C>A , CM000663.2:g.45500347C>A GRCh38
NC_000001.10:g.45966019C>A , CM000663.1:g.45966019C>A GRCh37
NC_000001.9:g.45738606C>A NCBI36
NG_013378.1:g.5164C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.15C>A MANE Select ENSP00000383840.4:p.Val5=
ENST00000401061.8:c.15C>A ENSP00000383840.4:p.Val5=
ENST00000616135.1:c.-157C>A ENSP00000478859.1:n.-157C>A
NM_015506.2:c.15C>A NP_056321.2:p.Val5=
XM_005270724.3:c.15C>A XP_005270781.1:p.Val5=
XM_011541204.1:c.-208C>A XP_011539506.1:n.-208C>A
NM_001330540.1:c.-208C>A NP_001317469.1:n.-208C>A
XM_005270724.5:c.15C>A XP_005270781.1:p.Val5=
NM_015506.3:c.15C>A MANE Select NP_056321.2:p.Val5=
NM_001330540.2:c.-208C>A NP_001317469.1:n.-208C>A