Canonical Allele Identifier: CA2244455700
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1910907428

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631807G>C , CM000679.2:g.4631807G>C GRCh38
NC_000017.10:g.4535102G>C , CM000679.1:g.4535102G>C GRCh37
NC_000017.9:g.4481851G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1810-28C>G MANE Select ENSP00000293761.3:n.1810-28C>G
ENST00000570836.6:c.1810-28C>G ENSP00000458832.1:n.1810-28C>G
ENST00000293761.7:c.1810-28C>G ENSP00000293761.3:n.1810-28C>G
ENST00000570836.5:c.1810-28C>G ENSP00000458832.1:n.1810-28C>G
ENST00000574640.1:c.1693-28C>G ENSP00000460483.1:n.1693-28C>G
NM_001140.3:c.1810-28C>G NP_001131.3:n.1810-28C>G
NM_001140.4:c.1810-28C>G NP_001131.3:n.1810-28C>G
NM_001140.5:c.1810-28C>G MANE Select NP_001131.3:n.1810-28C>G