Canonical Allele Identifier: CA2696092635
Gene: MMACHC HGNC NCBI

Linked Data

dbSNP Id: rs2149323774

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508775T>C , CM000663.2:g.45508775T>C GRCh38
NC_000001.10:g.45974447T>C , CM000663.1:g.45974447T>C GRCh37
NC_000001.9:g.45747034T>C NCBI36
NG_013378.1:g.13592T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.430-21T>C MANE Select ENSP00000383840.4:n.430-21T>C
ENST00000401061.8:c.430-21T>C ENSP00000383840.4:n.430-21T>C
ENST00000616135.1:c.259-21T>C ENSP00000478859.1:n.259-21T>C
NM_015506.2:c.430-21T>C NP_056321.2:n.430-21T>C
XM_005270724.3:c.235-21T>C XP_005270781.1:n.235-21T>C
XM_011541204.1:c.259-21T>C XP_011539506.1:n.259-21T>C
NM_001330540.1:c.259-21T>C NP_001317469.1:n.259-21T>C
XM_005270724.5:c.235-21T>C XP_005270781.1:n.235-21T>C
NM_015506.3:c.430-21T>C MANE Select NP_056321.2:n.430-21T>C
NM_001330540.2:c.259-21T>C NP_001317469.1:n.259-21T>C