Canonical Allele Identifier: CA2635534967
Gene: ALOX15 HGNC NCBI

Linked Data

gnomAD v4: 17-4631459-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631459C>T , CM000679.2:g.4631459C>T GRCh38
NC_000017.10:g.4534754C>T , CM000679.1:g.4534754C>T GRCh37
NC_000017.9:g.4481503C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293761.8:c.*141G>A MANE Select ENSP00000293761.3:n.*141G>A
ENST00000293761.7:c.*141G>A ENSP00000293761.3:n.*141G>A
ENST00000570836.5:c.*141G>A ENSP00000458832.1:n.*141G>A
ENST00000574640.1:c.*141G>A ENSP00000460483.1:n.*141G>A
NM_001140.3:c.*141G>A NP_001131.3:n.*141G>A
NM_001140.4:c.*141G>A NP_001131.3:n.*141G>A
NM_001140.5:c.*141G>A MANE Select NP_001131.3:n.*141G>A
Search 100 bp 5'
Search 100 bp 3'