Canonical Allele Identifier: CA697248261
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs762670287
gnomAD v3: 13-30731057-G-C
gnomAD v4: 13-30731057-G-C
MyVariant Identifiers: chr13:g.31305194G>C (hg19) chr13:g.30731057G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30731057G>C , CM000675.2:g.30731057G>C GRCh38
NC_000013.10:g.31305194G>C , CM000675.1:g.31305194G>C GRCh37
NC_000013.9:g.30203194G>C NCBI36
NG_011963.2:g.22580G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000617770.4:c.117-4494G>C ENSP00000479870.1:n.117-4494G>C
NM_001204406.1:c.117-4494G>C NP_001191335.1:n.117-4494G>C
NM_001204406.2:c.117-4494G>C NP_001191335.1:n.117-4494G>C
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