Canonical Allele Identifier: CA287132964
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs989156282
gnomAD v2: 17-4534865-G-A
gnomAD v4: 17-4631570-G-A
MyVariant Identifiers: chr17:g.4534865G>A (hg19) chr17:g.4631570G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631570G>A , CM000679.2:g.4631570G>A GRCh38
NC_000017.10:g.4534865G>A , CM000679.1:g.4534865G>A GRCh37
NC_000017.9:g.4481614G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*30C>T MANE Select ENSP00000293761.3:n.*30C>T
ENST00000570836.6:c.*30C>T ENSP00000458832.1:n.*30C>T
ENST00000293761.7:c.*30C>T ENSP00000293761.3:n.*30C>T
ENST00000570836.5:c.*30C>T ENSP00000458832.1:n.*30C>T
ENST00000574640.1:c.*30C>T ENSP00000460483.1:n.*30C>T
NM_001140.3:c.*30C>T NP_001131.3:n.*30C>T
NM_001140.4:c.*30C>T NP_001131.3:n.*30C>T
NM_001140.5:c.*30C>T MANE Select NP_001131.3:n.*30C>T
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