Canonical Allele Identifier: CA624591923
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1323667238
gnomAD v2: 17-4539409-G-A
gnomAD v3: 17-4636114-G-A
gnomAD v4: 17-4636114-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4636114G>A , CM000679.2:g.4636114G>A GRCh38
NC_000017.10:g.4539409G>A , CM000679.1:g.4539409G>A GRCh37
NC_000017.9:g.4486158G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.952-146C>T MANE Select ENSP00000293761.3:n.952-146C>T
ENST00000570836.6:c.952-146C>T ENSP00000458832.1:n.952-146C>T
ENST00000293761.7:c.952-146C>T ENSP00000293761.3:n.952-146C>T
ENST00000570836.5:c.952-146C>T ENSP00000458832.1:n.952-146C>T
ENST00000574640.1:c.835-146C>T ENSP00000460483.1:n.835-146C>T
NM_001140.3:c.952-146C>T NP_001131.3:n.952-146C>T
NM_001140.4:c.952-146C>T NP_001131.3:n.952-146C>T
NM_001140.5:c.952-146C>T MANE Select NP_001131.3:n.952-146C>T