Canonical Allele Identifier: CA980964841
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1910891968
gnomAD v3: 17-4631468-T-A
gnomAD v4: 17-4631468-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631468T>A , CM000679.2:g.4631468T>A GRCh38
NC_000017.10:g.4534763T>A , CM000679.1:g.4534763T>A GRCh37
NC_000017.9:g.4481512T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293761.8:c.*132A>T MANE Select ENSP00000293761.3:n.*132A>T
ENST00000293761.7:c.*132A>T ENSP00000293761.3:n.*132A>T
ENST00000570836.5:c.*132A>T ENSP00000458832.1:n.*132A>T
ENST00000574640.1:c.*132A>T ENSP00000460483.1:n.*132A>T
NM_001140.3:c.*132A>T NP_001131.3:n.*132A>T
NM_001140.4:c.*132A>T NP_001131.3:n.*132A>T
NM_001140.5:c.*132A>T MANE Select NP_001131.3:n.*132A>T