Canonical Allele Identifier: CA397246677
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1910906467
gnomAD v4: 17-4631780-C-T
MyVariant Identifiers: chr17:g.4535075C>T (hg19) chr17:g.4631780C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631780C>T , CM000679.2:g.4631780C>T GRCh38
NC_000017.10:g.4535075C>T , CM000679.1:g.4535075C>T GRCh37
NC_000017.9:g.4481824C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1810-1G>A MANE Select ENSP00000293761.3:n.1810-1G>A
ENST00000570836.6:c.1810-1G>A ENSP00000458832.1:n.1810-1G>A
ENST00000293761.7:c.1810-1G>A ENSP00000293761.3:n.1810-1G>A
ENST00000570836.5:c.1810-1G>A ENSP00000458832.1:n.1810-1G>A
ENST00000574640.1:c.1693-1G>A ENSP00000460483.1:n.1693-1G>A
NM_001140.3:c.1810-1G>A NP_001131.3:n.1810-1G>A
NM_001140.4:c.1810-1G>A NP_001131.3:n.1810-1G>A
NM_001140.5:c.1810-1G>A MANE Select NP_001131.3:n.1810-1G>A
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