Canonical Allele Identifier: CA697248190
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs1371670483
MyVariant Identifiers: chr13:g.31305059C>G (hg19) chr13:g.30730922C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30730922C>G , CM000675.2:g.30730922C>G GRCh38
NC_000013.10:g.31305059C>G , CM000675.1:g.31305059C>G GRCh37
NC_000013.9:g.30203059C>G NCBI36
NG_011963.2:g.22445C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000617770.4:c.117-4629C>G ENSP00000479870.1:n.117-4629C>G
NM_001204406.1:c.117-4629C>G NP_001191335.1:n.117-4629C>G
NM_001204406.2:c.117-4629C>G NP_001191335.1:n.117-4629C>G
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