Canonical Allele Identifier: CA522810634
Gene: MMACHC HGNC NCBI

Linked Data

dbSNP Id: rs1362990214
gnomAD v2: 1-45974430-G-A
gnomAD v3: 1-45508758-G-A
gnomAD v4: 1-45508758-G-A
MyVariant Identifiers: chr1:g.45974430G>A (hg19) chr1:g.45508758G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45508758G>A , CM000663.2:g.45508758G>A GRCh38
NC_000001.10:g.45974430G>A , CM000663.1:g.45974430G>A GRCh37
NC_000001.9:g.45747017G>A NCBI36
NG_013378.1:g.13575G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.430-38G>A MANE Select ENSP00000383840.4:n.430-38G>A
ENST00000401061.8:c.430-38G>A ENSP00000383840.4:n.430-38G>A
ENST00000616135.1:c.259-38G>A ENSP00000478859.1:n.259-38G>A
NM_015506.2:c.430-38G>A NP_056321.2:n.430-38G>A
XM_005270724.3:c.235-38G>A XP_005270781.1:n.235-38G>A
XM_011541204.1:c.259-38G>A XP_011539506.1:n.259-38G>A
NM_001330540.1:c.259-38G>A NP_001317469.1:n.259-38G>A
XM_005270724.5:c.235-38G>A XP_005270781.1:n.235-38G>A
NM_015506.3:c.430-38G>A MANE Select NP_056321.2:n.430-38G>A
NM_001330540.2:c.259-38G>A NP_001317469.1:n.259-38G>A
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