Canonical Allele Identifier: CA287132816
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs759165158
gnomAD v3: 17-4631199-T-G
gnomAD v4: 17-4631199-T-G
MyVariant Identifiers: chr17:g.4534494T>G (hg19) chr17:g.4631199T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631199T>G , CM000679.2:g.4631199T>G GRCh38
NC_000017.10:g.4534494T>G , CM000679.1:g.4534494T>G GRCh37
NC_000017.9:g.4481243T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*401A>C MANE Select ENSP00000293761.3:n.*401A>C
ENST00000293761.7:c.*401A>C ENSP00000293761.3:n.*401A>C
ENST00000570836.5:c.*401A>C ENSP00000458832.1:n.*401A>C
NM_001140.3:c.*401A>C NP_001131.3:n.*401A>C
NM_001140.4:c.*401A>C NP_001131.3:n.*401A>C
NM_001140.5:c.*401A>C MANE Select NP_001131.3:n.*401A>C
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