Canonical Allele Identifier: CA247372920
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs948470994
MyVariant Identifiers: chr13:g.31305103G>A (hg19) chr13:g.30730966G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30730966G>A , CM000675.2:g.30730966G>A GRCh38
NC_000013.10:g.31305103G>A , CM000675.1:g.31305103G>A GRCh37
NC_000013.9:g.30203103G>A NCBI36
NG_011963.2:g.22489G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000617770.4:c.117-4585G>A ENSP00000479870.1:n.117-4585G>A
NM_001204406.1:c.117-4585G>A NP_001191335.1:n.117-4585G>A
NM_001204406.2:c.117-4585G>A NP_001191335.1:n.117-4585G>A
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