Canonical Allele Identifier: CA697248227
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs1268170792
MyVariant Identifiers: chr13:g.31305104T>C (hg19) chr13:g.30730967T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30730967T>C , CM000675.2:g.30730967T>C GRCh38
NC_000013.10:g.31305104T>C , CM000675.1:g.31305104T>C GRCh37
NC_000013.9:g.30203104T>C NCBI36
NG_011963.2:g.22490T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000617770.4:c.117-4584T>C ENSP00000479870.1:n.117-4584T>C
NM_001204406.1:c.117-4584T>C NP_001191335.1:n.117-4584T>C
NM_001204406.2:c.117-4584T>C NP_001191335.1:n.117-4584T>C
Search 100 bp 5'
Search 100 bp 3'