Canonical Allele Identifier: CA2082068768
Gene: ALOX5AP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30729828G= , CM000675.2:g.30729828G= GRCh38
NC_000013.10:g.31303965G= , CM000675.1:g.31303965G= GRCh37
NC_000013.9:g.30201965G= NCBI36
NG_011963.2:g.21351G=

Transcript Alleles

HGVS Amino-acid Change
NM_001204406.1:c.117-5723G= NP_001191335.1:n.117-5723G=
NM_001204406.2:c.117-5723G= NP_001191335.1:n.117-5723G=
ENST00000617770.4:c.117-5723G= ENSP00000479870.1:n.117-5723G=