Canonical Allele Identifier: CA2635535064
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs2150534319
gnomAD v4: 17-4631599-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631599C>T , CM000679.2:g.4631599C>T GRCh38
NC_000017.10:g.4534894C>T , CM000679.1:g.4534894C>T GRCh37
NC_000017.9:g.4481643C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*1G>A MANE Select ENSP00000293761.3:n.*1G>A
ENST00000570836.6:c.*1G>A ENSP00000458832.1:n.*1G>A
ENST00000293761.7:c.*1G>A ENSP00000293761.3:n.*1G>A
ENST00000570836.5:c.*1G>A ENSP00000458832.1:n.*1G>A
ENST00000574640.1:c.*1G>A ENSP00000460483.1:n.*1G>A
NM_001140.3:c.*1G>A NP_001131.3:n.*1G>A
NM_001140.4:c.*1G>A NP_001131.3:n.*1G>A
NM_001140.5:c.*1G>A MANE Select NP_001131.3:n.*1G>A
Search 100 bp 5'
Search 100 bp 3'