Canonical Allele Identifier: CA2082069308

Gene: ALOX5AP

Linked Data

• dbSNP Id: rs753906497

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.30730929T>C , CM000675.2:g.30730929T>C	GRCh38
NC_000013.10:g.31305066T>C , CM000675.1:g.31305066T>C	GRCh37
NC_000013.9:g.30203066T>C	NCBI36
NG_011963.2:g.22452T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000617770.4:c.117-4622T>C	ENSP00000479870.1:n.117-4622T>C
NM_001204406.1:c.117-4622T>C	NP_001191335.1:n.117-4622T>C
NM_001204406.2:c.117-4622T>C	NP_001191335.1:n.117-4622T>C