Canonical Allele Identifier: CA340128261
Gene: MMACHC HGNC NCBI

Linked Data

dbSNP Id: rs1454919873

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500336G>A , CM000663.2:g.45500336G>A GRCh38
NC_000001.10:g.45966008G>A , CM000663.1:g.45966008G>A GRCh37
NC_000001.9:g.45738595G>A NCBI36
NG_013378.1:g.5153G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.4G>A MANE Select ENSP00000383840.4:p.Glu2Lys
ENST00000401061.8:c.4G>A ENSP00000383840.4:p.Glu2Lys
NM_015506.2:c.4G>A NP_056321.2:p.Glu2Lys
XM_005270724.3:c.4G>A XP_005270781.1:p.Glu2Lys
XM_011541204.1:c.-219G>A XP_011539506.1:n.-219G>A
NM_001330540.1:c.-219G>A NP_001317469.1:n.-219G>A
XM_005270724.5:c.4G>A XP_005270781.1:p.Glu2Lys
NM_015506.3:c.4G>A MANE Select NP_056321.2:p.Glu2Lys
NM_001330540.2:c.-219G>A NP_001317469.1:n.-219G>A