Canonical Allele Identifier: CA697248224
Gene: ALOX5AP HGNC NCBI

Linked Data

dbSNP Id: rs1275098194
gnomAD v3: 13-30730955-C-T
gnomAD v4: 13-30730955-C-T
MyVariant Identifiers: chr13:g.31305092C>T (hg19) chr13:g.30730955C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30730955C>T , CM000675.2:g.30730955C>T GRCh38
NC_000013.10:g.31305092C>T , CM000675.1:g.31305092C>T GRCh37
NC_000013.9:g.30203092C>T NCBI36
NG_011963.2:g.22478C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000617770.4:c.117-4596C>T ENSP00000479870.1:n.117-4596C>T
NM_001204406.1:c.117-4596C>T NP_001191335.1:n.117-4596C>T
NM_001204406.2:c.117-4596C>T NP_001191335.1:n.117-4596C>T
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