Canonical Allele Identifier: CA2082069266
Gene: ALOX5AP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30730827T= , CM000675.2:g.30730827T= GRCh38
NC_000013.10:g.31304964T= , CM000675.1:g.31304964T= GRCh37
NC_000013.9:g.30202964T= NCBI36
NG_011963.2:g.22350T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617770.4:c.117-4724T= ENSP00000479870.1:n.117-4724T=
NM_001204406.1:c.117-4724T= NP_001191335.1:n.117-4724T=
NM_001204406.2:c.117-4724T= NP_001191335.1:n.117-4724T=