Canonical Allele Identifier: CA2082069319
Gene: ALOX5AP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30730950T= , CM000675.2:g.30730950T= GRCh38
NC_000013.10:g.31305087T= , CM000675.1:g.31305087T= GRCh37
NC_000013.9:g.30203087T= NCBI36
NG_011963.2:g.22473T=

Transcript Alleles

HGVS Amino-acid change
ENST00000617770.4:c.117-4601T= ENSP00000479870.1:n.117-4601T=
NM_001204406.1:c.117-4601T= NP_001191335.1:n.117-4601T=
NM_001204406.2:c.117-4601T= NP_001191335.1:n.117-4601T=