Canonical Allele Identifier: CA2244455491
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1910889217
gnomAD v4: 17-4631381-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631381A>G , CM000679.2:g.4631381A>G GRCh38
NC_000017.10:g.4534676A>G , CM000679.1:g.4534676A>G GRCh37
NC_000017.9:g.4481425A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*219T>C MANE Select ENSP00000293761.3:n.*219T>C
ENST00000293761.7:c.*219T>C ENSP00000293761.3:n.*219T>C
ENST00000570836.5:c.*219T>C ENSP00000458832.1:n.*219T>C
ENST00000574640.1:c.*219T>C ENSP00000460483.1:n.*219T>C
NM_001140.3:c.*219T>C NP_001131.3:n.*219T>C
NM_001140.4:c.*219T>C NP_001131.3:n.*219T>C
NM_001140.5:c.*219T>C MANE Select NP_001131.3:n.*219T>C