Canonical Allele Identifier: CA980964817
Gene: ALOX15 HGNC NCBI

Linked Data

gnomAD v3: 17-4631186-G-C
gnomAD v4: 17-4631186-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631186G>C , CM000679.2:g.4631186G>C GRCh38
NC_000017.10:g.4534481G>C , CM000679.1:g.4534481G>C GRCh37
NC_000017.9:g.4481230G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*414C>G MANE Select ENSP00000293761.3:n.*414C>G
ENST00000293761.7:c.*414C>G ENSP00000293761.3:n.*414C>G
ENST00000570836.5:c.*414C>G ENSP00000458832.1:n.*414C>G
NM_001140.3:c.*414C>G NP_001131.3:n.*414C>G
NM_001140.4:c.*414C>G NP_001131.3:n.*414C>G
NM_001140.5:c.*414C>G MANE Select NP_001131.3:n.*414C>G
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