Canonical Allele Identifier: CA697248223
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs1484657119
gnomAD v3: 13-30730954-T-A
gnomAD v4: 13-30730954-T-A
MyVariant Identifiers: chr13:g.31305091T>A (hg19) chr13:g.30730954T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30730954T>A , CM000675.2:g.30730954T>A GRCh38
NC_000013.10:g.31305091T>A , CM000675.1:g.31305091T>A GRCh37
NC_000013.9:g.30203091T>A NCBI36
NG_011963.2:g.22477T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000617770.4:c.117-4597T>A ENSP00000479870.1:n.117-4597T>A
NM_001204406.1:c.117-4597T>A NP_001191335.1:n.117-4597T>A
NM_001204406.2:c.117-4597T>A NP_001191335.1:n.117-4597T>A
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