Canonical Allele Identifier: CA2082069329
Gene: ALOX5AP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30730966G= , CM000675.2:g.30730966G= GRCh38
NC_000013.10:g.31305103G= , CM000675.1:g.31305103G= GRCh37
NC_000013.9:g.30203103G= NCBI36
NG_011963.2:g.22489G=

Transcript Alleles

HGVS Amino-acid change
ENST00000617770.4:c.117-4585G= ENSP00000479870.1:n.117-4585G=
NM_001204406.1:c.117-4585G= NP_001191335.1:n.117-4585G=
NM_001204406.2:c.117-4585G= NP_001191335.1:n.117-4585G=