Canonical Allele Identifier: CA697248221
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs1208732819
gnomAD v3: 13-30730950-T-C
gnomAD v4: 13-30730950-T-C
MyVariant Identifiers: chr13:g.31305087T>C (hg19) chr13:g.30730950T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30730950T>C , CM000675.2:g.30730950T>C GRCh38
NC_000013.10:g.31305087T>C , CM000675.1:g.31305087T>C GRCh37
NC_000013.9:g.30203087T>C NCBI36
NG_011963.2:g.22473T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000617770.4:c.117-4601T>C ENSP00000479870.1:n.117-4601T>C
NM_001204406.1:c.117-4601T>C NP_001191335.1:n.117-4601T>C
NM_001204406.2:c.117-4601T>C NP_001191335.1:n.117-4601T>C
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