Canonical Allele Identifier: CA247372908
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs916958762
gnomAD v3: 13-30730958-A-G
gnomAD v4: 13-30730958-A-G
MyVariant Identifiers: chr13:g.31305095A>G (hg19) chr13:g.30730958A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30730958A>G , CM000675.2:g.30730958A>G GRCh38
NC_000013.10:g.31305095A>G , CM000675.1:g.31305095A>G GRCh37
NC_000013.9:g.30203095A>G NCBI36
NG_011963.2:g.22481A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000617770.4:c.117-4593A>G ENSP00000479870.1:n.117-4593A>G
NM_001204406.1:c.117-4593A>G NP_001191335.1:n.117-4593A>G
NM_001204406.2:c.117-4593A>G NP_001191335.1:n.117-4593A>G
Search 100 bp 5'
Search 100 bp 3'