Canonical Allele Identifier: CA247372900
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs753906497
gnomAD v3: 13-30730929-T-G
gnomAD v4: 13-30730929-T-G
MyVariant Identifiers: chr13:g.31305066T>G (hg19) chr13:g.30730929T>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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