Canonical Allele Identifier: CA13784446
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs4076128

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30731006A>G , CM000675.2:g.30731006A>G GRCh38
NC_000013.10:g.31305143A>G , CM000675.1:g.31305143A>G GRCh37
NC_000013.9:g.30203143A>G NCBI36
NG_011963.2:g.22529A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000617770.4:c.117-4545A>G ENSP00000479870.1:n.117-4545A>G
NM_001204406.1:c.117-4545A>G NP_001191335.1:n.117-4545A>G
NM_001204406.2:c.117-4545A>G NP_001191335.1:n.117-4545A>G