Canonical Allele Identifier: CA772437301
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1358898896

Genomic Alleles

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

Transcript Alleles

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