Canonical Allele Identifier: CA954573119
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs1951738562
gnomAD v3: 13-30738584-G-C
gnomAD v4: 13-30738584-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30738584G>C , CM000675.2:g.30738584G>C GRCh38
NC_000013.10:g.31312721G>C , CM000675.1:g.31312721G>C GRCh37
NC_000013.9:g.30210721G>C NCBI36
NG_011963.2:g.30107G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000380490.5:c.70+2909G>C MANE Select ENSP00000369858.3:n.70+2909G>C
ENST00000380490.4:c.70+2909G>C ENSP00000369858.3:n.70+2909G>C
ENST00000617770.4:c.241+2909G>C ENSP00000479870.1:n.241+2909G>C
NM_001204406.1:c.241+2909G>C NP_001191335.1:n.241+2909G>C
NM_001629.3:c.70+2909G>C NP_001620.2:n.70+2909G>C
XM_011535024.1:c.70+2909G>C XP_011533326.1:n.70+2909G>C
NM_001204406.2:c.241+2909G>C NP_001191335.1:n.241+2909G>C
NM_001629.4:c.70+2909G>C MANE Select NP_001620.2:n.70+2909G>C
Search 100 bp 5'
Search 100 bp 3'