Canonical Allele Identifier: CA954568335
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs1951675984
gnomAD v3: 13-30730919-G-A
gnomAD v4: 13-30730919-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30730919G>A , CM000675.2:g.30730919G>A GRCh38
NC_000013.10:g.31305056G>A , CM000675.1:g.31305056G>A GRCh37
NC_000013.9:g.30203056G>A NCBI36
NG_011963.2:g.22442G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000617770.4:c.117-4632G>A ENSP00000479870.1:n.117-4632G>A
NM_001204406.1:c.117-4632G>A NP_001191335.1:n.117-4632G>A
NM_001204406.2:c.117-4632G>A NP_001191335.1:n.117-4632G>A
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