Canonical Allele Identifier: CA624591157
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1189426706
gnomAD v2: 17-4534479-A-T
gnomAD v3: 17-4631184-A-T
gnomAD v4: 17-4631184-A-T
MyVariant Identifiers: chr17:g.4534479A>T (hg19) chr17:g.4631184A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631184A>T , CM000679.2:g.4631184A>T GRCh38
NC_000017.10:g.4534479A>T , CM000679.1:g.4534479A>T GRCh37
NC_000017.9:g.4481228A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*416T>A MANE Select ENSP00000293761.3:n.*416T>A
ENST00000293761.7:c.*416T>A ENSP00000293761.3:n.*416T>A
ENST00000570836.5:c.*416T>A ENSP00000458832.1:n.*416T>A
NM_001140.3:c.*416T>A NP_001131.3:n.*416T>A
NM_001140.4:c.*416T>A NP_001131.3:n.*416T>A
NM_001140.5:c.*416T>A MANE Select NP_001131.3:n.*416T>A
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