Canonical Allele Identifier: CA2244455521
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1358898896
gnomAD v3: 17-4631445-G-A
gnomAD v4: 17-4631445-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631445G>A , CM000679.2:g.4631445G>A GRCh38
NC_000017.10:g.4534740G>A , CM000679.1:g.4534740G>A GRCh37
NC_000017.9:g.4481489G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293761.8:c.*155C>T MANE Select ENSP00000293761.3:n.*155C>T
ENST00000293761.7:c.*155C>T ENSP00000293761.3:n.*155C>T
ENST00000570836.5:c.*155C>T ENSP00000458832.1:n.*155C>T
ENST00000574640.1:c.*155C>T ENSP00000460483.1:n.*155C>T
NM_001140.3:c.*155C>T NP_001131.3:n.*155C>T
NM_001140.4:c.*155C>T NP_001131.3:n.*155C>T
NM_001140.5:c.*155C>T MANE Select NP_001131.3:n.*155C>T