Canonical Allele Identifier: CA287132798
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs78305230
MyVariant Identifiers: chr17:g.4534439A>C (hg19) chr17:g.4631144A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631144A>C , CM000679.2:g.4631144A>C GRCh38
NC_000017.10:g.4534439A>C , CM000679.1:g.4534439A>C GRCh37
NC_000017.9:g.4481188A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*456T>G MANE Select ENSP00000293761.3:n.*456T>G
ENST00000293761.7:c.*456T>G ENSP00000293761.3:n.*456T>G
ENST00000570836.5:c.*456T>G ENSP00000458832.1:n.*456T>G
NM_001140.3:c.*456T>G NP_001131.3:n.*456T>G
NM_001140.4:c.*456T>G NP_001131.3:n.*456T>G
NM_001140.5:c.*456T>G MANE Select NP_001131.3:n.*456T>G
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