Canonical Allele Identifier: CA624854358
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1429698654
gnomAD v2: 17-4534769-G-T
gnomAD v3: 17-4631474-G-T
gnomAD v4: 17-4631474-G-T
MyVariant Identifiers: chr17:g.4534769G>T (hg19) chr17:g.4631474G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631474G>T , CM000679.2:g.4631474G>T GRCh38
NC_000017.10:g.4534769G>T , CM000679.1:g.4534769G>T GRCh37
NC_000017.9:g.4481518G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*126C>A MANE Select ENSP00000293761.3:n.*126C>A
ENST00000293761.7:c.*126C>A ENSP00000293761.3:n.*126C>A
ENST00000570836.5:c.*126C>A ENSP00000458832.1:n.*126C>A
ENST00000574640.1:c.*126C>A ENSP00000460483.1:n.*126C>A
NM_001140.3:c.*126C>A NP_001131.3:n.*126C>A
NM_001140.4:c.*126C>A NP_001131.3:n.*126C>A
NM_001140.5:c.*126C>A MANE Select NP_001131.3:n.*126C>A
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