Canonical Allele Identifier: CA14369205
Gene: ALOX15 HGNC NCBI
COSMIC:
COSN6657501 (not active)
MyVariant.info:
GRCh38 chr17:g.4636097C>T
GRCh37 chr17:g.4539392C>T
gnomAD v2:
17:4539392 C / T
gnomAD v3:
17:4636097 C / T
gnomAD v4:
chr17-4636097-C-T
Joint Max Group AF 0.5964406 (EAS)
Genomes Max Group AF 0.60257346 (EAS)
Exomes Max Group AF 0.5932075 (EAS)
dbSNP:
7217186
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4636097C>T , CM000679.2:g.4636097C>T GRCh38
NC_000017.10:g.4539392C>T , CM000679.1:g.4539392C>T GRCh37
NC_000017.9:g.4486141C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.952-129G>A MANE Select ENSP00000293761.3:n.952-129G>A
ENST00000570836.6:c.952-129G>A ENSP00000458832.1:n.952-129G>A
ENST00000293761.7:c.952-129G>A ENSP00000293761.3:n.952-129G>A
ENST00000570836.5:c.952-129G>A ENSP00000458832.1:n.952-129G>A
ENST00000574640.1:c.835-129G>A ENSP00000460483.1:n.835-129G>A
NM_001140.3:c.952-129G>A NP_001131.3:n.952-129G>A
NM_001140.4:c.952-129G>A NP_001131.3:n.952-129G>A
NM_001140.5:c.952-129G>A MANE Select NP_001131.3:n.952-129G>A
Search 100 bp 5'
Search 100 bp 3'