Canonical Allele Identifier: CA2473783623
Gene: MMACHC HGNC NCBI

Linked Data

dbSNP Id: rs1643675803
gnomAD v4: 1-45508762-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508762T>G , CM000663.2:g.45508762T>G GRCh38
NC_000001.10:g.45974434T>G , CM000663.1:g.45974434T>G GRCh37
NC_000001.9:g.45747021T>G NCBI36
NG_013378.1:g.13579T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.430-34T>G MANE Select ENSP00000383840.4:n.430-34T>G
ENST00000401061.8:c.430-34T>G ENSP00000383840.4:n.430-34T>G
ENST00000616135.1:c.259-34T>G ENSP00000478859.1:n.259-34T>G
NM_015506.2:c.430-34T>G NP_056321.2:n.430-34T>G
XM_005270724.3:c.235-34T>G XP_005270781.1:n.235-34T>G
XM_011541204.1:c.259-34T>G XP_011539506.1:n.259-34T>G
NM_001330540.1:c.259-34T>G NP_001317469.1:n.259-34T>G
XM_005270724.5:c.235-34T>G XP_005270781.1:n.235-34T>G
NM_015506.3:c.430-34T>G MANE Select NP_056321.2:n.430-34T>G
NM_001330540.2:c.259-34T>G NP_001317469.1:n.259-34T>G