Canonical Allele Identifier: CA2082069255
Gene: ALOX5AP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30730815T= , CM000675.2:g.30730815T= GRCh38
NC_000013.10:g.31304952T= , CM000675.1:g.31304952T= GRCh37
NC_000013.9:g.30202952T= NCBI36
NG_011963.2:g.22338T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000617770.4:c.117-4736T= ENSP00000479870.1:n.117-4736T=
NM_001204406.1:c.117-4736T= NP_001191335.1:n.117-4736T=
NM_001204406.2:c.117-4736T= NP_001191335.1:n.117-4736T=