Canonical Allele Identifier: CA772437423
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1351645557
gnomAD v3: 17-4631548-T-C
gnomAD v4: 17-4631548-T-C
MyVariant Identifiers: chr17:g.4534843T>C (hg19) chr17:g.4631548T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631548T>C , CM000679.2:g.4631548T>C GRCh38
NC_000017.10:g.4534843T>C , CM000679.1:g.4534843T>C GRCh37
NC_000017.9:g.4481592T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293761.8:c.*52A>G MANE Select ENSP00000293761.3:n.*52A>G
ENST00000570836.6:c.*52A>G ENSP00000458832.1:n.*52A>G
ENST00000293761.7:c.*52A>G ENSP00000293761.3:n.*52A>G
ENST00000570836.5:c.*52A>G ENSP00000458832.1:n.*52A>G
ENST00000574640.1:c.*52A>G ENSP00000460483.1:n.*52A>G
NM_001140.3:c.*52A>G NP_001131.3:n.*52A>G
NM_001140.4:c.*52A>G NP_001131.3:n.*52A>G
NM_001140.5:c.*52A>G MANE Select NP_001131.3:n.*52A>G
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