Canonical Allele Identifier: CA2082069265
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs1951675371
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30730826C>A , CM000675.2:g.30730826C>A GRCh38
NC_000013.10:g.31304963C>A , CM000675.1:g.31304963C>A GRCh37
NC_000013.9:g.30202963C>A NCBI36
NG_011963.2:g.22349C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000617770.4:c.117-4725C>A ENSP00000479870.1:n.117-4725C>A
NM_001204406.1:c.117-4725C>A NP_001191335.1:n.117-4725C>A
NM_001204406.2:c.117-4725C>A NP_001191335.1:n.117-4725C>A
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