Canonical Allele Identifier: CA697252460
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs1232438690
MyVariant Identifiers: chr13:g.31312763T>A (hg19) chr13:g.30738626T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30738626T>A , CM000675.2:g.30738626T>A GRCh38
NC_000013.10:g.31312763T>A , CM000675.1:g.31312763T>A GRCh37
NC_000013.9:g.30210763T>A NCBI36
NG_011963.2:g.30149T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000380490.5:c.70+2951T>A MANE Select ENSP00000369858.3:n.70+2951T>A
ENST00000380490.4:c.70+2951T>A ENSP00000369858.3:n.70+2951T>A
ENST00000617770.4:c.241+2951T>A ENSP00000479870.1:n.241+2951T>A
NM_001204406.1:c.241+2951T>A NP_001191335.1:n.241+2951T>A
NM_001629.3:c.70+2951T>A NP_001620.2:n.70+2951T>A
XM_011535024.1:c.70+2951T>A XP_011533326.1:n.70+2951T>A
NM_001204406.2:c.241+2951T>A NP_001191335.1:n.241+2951T>A
NM_001629.4:c.70+2951T>A MANE Select NP_001620.2:n.70+2951T>A
Search 100 bp 5'
Search 100 bp 3'