Canonical Allele Identifier: CA2244455589
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1597428447
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631574C>G , CM000679.2:g.4631574C>G GRCh38
NC_000017.10:g.4534869C>G , CM000679.1:g.4534869C>G GRCh37
NC_000017.9:g.4481618C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*26G>C MANE Select ENSP00000293761.3:n.*26G>C
ENST00000570836.6:c.*26G>C ENSP00000458832.1:n.*26G>C
ENST00000293761.7:c.*26G>C ENSP00000293761.3:n.*26G>C
ENST00000570836.5:c.*26G>C ENSP00000458832.1:n.*26G>C
ENST00000574640.1:c.*26G>C ENSP00000460483.1:n.*26G>C
NM_001140.3:c.*26G>C NP_001131.3:n.*26G>C
NM_001140.4:c.*26G>C NP_001131.3:n.*26G>C
NM_001140.5:c.*26G>C MANE Select NP_001131.3:n.*26G>C
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