Canonical Allele Identifier: CA772437115
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1181697905
gnomAD v3: 17-4631150-G-A
gnomAD v4: 17-4631150-G-A
MyVariant Identifiers: chr17:g.4534445G>A (hg19) chr17:g.4631150G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631150G>A , CM000679.2:g.4631150G>A GRCh38
NC_000017.10:g.4534445G>A , CM000679.1:g.4534445G>A GRCh37
NC_000017.9:g.4481194G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*450C>T MANE Select ENSP00000293761.3:n.*450C>T
ENST00000293761.7:c.*450C>T ENSP00000293761.3:n.*450C>T
ENST00000570836.5:c.*450C>T ENSP00000458832.1:n.*450C>T
NM_001140.3:c.*450C>T NP_001131.3:n.*450C>T
NM_001140.4:c.*450C>T NP_001131.3:n.*450C>T
NM_001140.5:c.*450C>T MANE Select NP_001131.3:n.*450C>T
Search 100 bp 5'
Search 100 bp 3'