Canonical Allele Identifier: CA624591163
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1339948727
gnomAD v2: 17-4534611-T-A
MyVariant Identifiers: chr17:g.4534611T>A (hg19) chr17:g.4631316T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631316T>A , CM000679.2:g.4631316T>A GRCh38
NC_000017.10:g.4534611T>A , CM000679.1:g.4534611T>A GRCh37
NC_000017.9:g.4481360T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*284A>T MANE Select ENSP00000293761.3:n.*284A>T
ENST00000293761.7:c.*284A>T ENSP00000293761.3:n.*284A>T
ENST00000570836.5:c.*284A>T ENSP00000458832.1:n.*284A>T
NM_001140.3:c.*284A>T NP_001131.3:n.*284A>T
NM_001140.4:c.*284A>T NP_001131.3:n.*284A>T
NM_001140.5:c.*284A>T MANE Select NP_001131.3:n.*284A>T
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