Canonical Allele Identifier: CA287132813
Gene: ALOX15 HGNC NCBI

Linked Data

dbSNP Id: rs1023907609
gnomAD v2: 17-4534491-C-T
gnomAD v3: 17-4631196-C-T
gnomAD v4: 17-4631196-C-T
MyVariant Identifiers: chr17:g.4534491C>T (hg19) chr17:g.4631196C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4631196C>T , CM000679.2:g.4631196C>T GRCh38
NC_000017.10:g.4534491C>T , CM000679.1:g.4534491C>T GRCh37
NC_000017.9:g.4481240C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000293761.8:c.*404G>A MANE Select ENSP00000293761.3:n.*404G>A
ENST00000293761.7:c.*404G>A ENSP00000293761.3:n.*404G>A
ENST00000570836.5:c.*404G>A ENSP00000458832.1:n.*404G>A
NM_001140.3:c.*404G>A NP_001131.3:n.*404G>A
NM_001140.4:c.*404G>A NP_001131.3:n.*404G>A
NM_001140.5:c.*404G>A MANE Select NP_001131.3:n.*404G>A
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