Canonical Allele Identifier: CA772437150
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1277750593
gnomAD v4: 17-4631179-T-C
MyVariant Identifiers: chr17:g.4534474T>C (hg19) chr17:g.4631179T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631179T>C , CM000679.2:g.4631179T>C GRCh38
NC_000017.10:g.4534474T>C , CM000679.1:g.4534474T>C GRCh37
NC_000017.9:g.4481223T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*421A>G MANE Select ENSP00000293761.3:n.*421A>G
ENST00000293761.7:c.*421A>G ENSP00000293761.3:n.*421A>G
ENST00000570836.5:c.*421A>G ENSP00000458832.1:n.*421A>G
NM_001140.3:c.*421A>G NP_001131.3:n.*421A>G
NM_001140.4:c.*421A>G NP_001131.3:n.*421A>G
NM_001140.5:c.*421A>G MANE Select NP_001131.3:n.*421A>G
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