Canonical Allele Identifier: CA287132933
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs905495926
gnomAD v4: 17-4631540-C-G
MyVariant Identifiers: chr17:g.4631540C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631540C>G , CM000679.2:g.4631540C>G GRCh38
NC_000017.10:g.4534835C>G , CM000679.1:g.4534835C>G GRCh37
NC_000017.9:g.4481584C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000293761.8:c.*60G>C MANE Select ENSP00000293761.3:n.*60G>C
ENST00000570836.6:c.*60G>C ENSP00000458832.1:n.*60G>C
ENST00000293761.7:c.*60G>C ENSP00000293761.3:n.*60G>C
ENST00000570836.5:c.*60G>C ENSP00000458832.1:n.*60G>C
ENST00000574640.1:c.*60G>C ENSP00000460483.1:n.*60G>C
NM_001140.3:c.*60G>C NP_001131.3:n.*60G>C
NM_001140.4:c.*60G>C NP_001131.3:n.*60G>C
NM_001140.5:c.*60G>C MANE Select NP_001131.3:n.*60G>C
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