Canonical Allele Identifier: CA13784444
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs17216473

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000617770.4:c.117-5723G>A ENSP00000479870.1:n.117-5723G>A
NM_001204406.1:c.117-5723G>A NP_001191335.1:n.117-5723G>A
NM_001204406.2:c.117-5723G>A NP_001191335.1:n.117-5723G>A