Canonical Allele Identifier: CA2505092639
Gene: DHODH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.72024647A>G , CM000678.2:g.72024647A>G GRCh38
NC_000016.9:g.72058546A>G , CM000678.1:g.72058546A>G GRCh37
NC_000016.8:g.70616047A>G NCBI36
NG_016271.1:g.20904A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000219240.9:c.*448A>G MANE Select ENSP00000219240.4:n.*448A>G
ENST00000219240.8:c.*448A>G ENSP00000219240.4:n.*448A>G
ENST00000572887.5:c.*448A>G ENSP00000461848.1:n.*448A>G
NM_001361.4:c.*448A>G NP_001352.2:n.*448A>G
XM_005255827.4:c.*448A>G XP_005255884.1:n.*448A>G
XM_005255829.4:c.*448A>G XP_005255886.1:n.*448A>G
XM_017022990.2:c.*448A>G XP_016878479.1:n.*448A>G
NM_001361.5:c.*448A>G MANE Select NP_001352.2:n.*448A>G
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