Canonical Allele Identifier: CA2082069315
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs1951676126

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30730946C>G , CM000675.2:g.30730946C>G GRCh38
NC_000013.10:g.31305083C>G , CM000675.1:g.31305083C>G GRCh37
NC_000013.9:g.30203083C>G NCBI36
NG_011963.2:g.22469C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000617770.4:c.117-4605C>G ENSP00000479870.1:n.117-4605C>G
NM_001204406.1:c.117-4605C>G NP_001191335.1:n.117-4605C>G
NM_001204406.2:c.117-4605C>G NP_001191335.1:n.117-4605C>G