Canonical Allele Identifier: CA287137290
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1030552082
gnomAD v2: 17-4539546-A-C
gnomAD v3: 17-4636251-A-C
gnomAD v4: 17-4636251-A-C
MyVariant Identifiers: chr17:g.4539546A>C (hg19) chr17:g.4636251A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4636251A>C , CM000679.2:g.4636251A>C GRCh38
NC_000017.10:g.4539546A>C , CM000679.1:g.4539546A>C GRCh37
NC_000017.9:g.4486295A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.952-283T>G MANE Select ENSP00000293761.3:n.952-283T>G
ENST00000570836.6:c.952-283T>G ENSP00000458832.1:n.952-283T>G
ENST00000293761.7:c.952-283T>G ENSP00000293761.3:n.952-283T>G
ENST00000570836.5:c.952-283T>G ENSP00000458832.1:n.952-283T>G
ENST00000574640.1:c.835-283T>G ENSP00000460483.1:n.835-283T>G
NM_001140.3:c.952-283T>G NP_001131.3:n.952-283T>G
NM_001140.4:c.952-283T>G NP_001131.3:n.952-283T>G
NM_001140.5:c.952-283T>G MANE Select NP_001131.3:n.952-283T>G
Search 100 bp 5'
Search 100 bp 3'