Canonical Allele Identifier: CA8306721
Gene: ALOX15 HGNC NCBI
COSMIC:
COSN6657498 (not active)
MyVariant.info:
GRCh38 chr17:g.4632090A>G
GRCh37 chr17:g.4535385A>G
gnomAD v2:
17:4535385 A / G
gnomAD v3:
17:4632090 A / G
gnomAD v4:
chr17-4632090-A-G
Joint Max Group AF 0.57986768 (EAS)
Genomes Max Group AF 0.56300995 (EAS)
Exomes Max Group AF 0.58020312 (EAS)
dbSNP:
2619112
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4632090A>G , CM000679.2:g.4632090A>G GRCh38
NC_000017.10:g.4535385A>G , CM000679.1:g.4535385A>G GRCh37
NC_000017.9:g.4482134A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.1642-34T>C MANE Select ENSP00000293761.3:n.1642-34T>C
ENST00000570836.6:c.1642-34T>C ENSP00000458832.1:n.1642-34T>C
ENST00000293761.7:c.1642-34T>C ENSP00000293761.3:n.1642-34T>C
ENST00000570836.5:c.1642-34T>C ENSP00000458832.1:n.1642-34T>C
ENST00000574640.1:c.1525-34T>C ENSP00000460483.1:n.1525-34T>C
NM_001140.3:c.1642-34T>C NP_001131.3:n.1642-34T>C
NM_001140.4:c.1642-34T>C NP_001131.3:n.1642-34T>C
NM_001140.5:c.1642-34T>C MANE Select NP_001131.3:n.1642-34T>C
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