Canonical Allele Identifier: CA21828801
Gene: MMACHC HGNC NCBI

Linked Data

dbSNP Id: rs933447358
gnomAD v4: 1-45507392-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45507392C>T , CM000663.2:g.45507392C>T GRCh38
NC_000001.10:g.45973064C>T , CM000663.1:g.45973064C>T GRCh37
NC_000001.9:g.45745651C>T NCBI36
NG_013378.1:g.12209C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.118C>T MANE Select ENSP00000383840.4:p.His40Tyr
ENST00000401061.8:c.118C>T ENSP00000383840.4:p.His40Tyr
ENST00000616135.1:c.-54C>T ENSP00000478859.1:n.-54C>T
NM_015506.2:c.118C>T NP_056321.2:p.His40Tyr
XM_005270724.3:c.82-820C>T XP_005270781.1:n.82-820C>T
XM_011541204.1:c.-54C>T XP_011539506.1:n.-54C>T
NM_001330540.1:c.-54C>T NP_001317469.1:n.-54C>T
XM_005270724.5:c.82-820C>T XP_005270781.1:n.82-820C>T
NM_015506.3:c.118C>T MANE Select NP_056321.2:p.His40Tyr
NM_001330540.2:c.-54C>T NP_001317469.1:n.-54C>T