Canonical Allele Identifier: CA2082066717
Community Standard Title: NC_000013.11:g.30725416G=
Gene: ALOX5AP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.30725416G= , CM000675.2:g.30725416G= GRCh38
NC_000013.10:g.31299553G= , CM000675.1:g.31299553G= GRCh37
NC_000013.9:g.30197553G= NCBI36
NG_011963.2:g.16939G=

Transcript Alleles

HGVS Amino-acid Change
NM_001204406.1:c.117-10135G= NP_001191335.1:n.117-10135G=
NM_001204406.2:c.117-10135G= NP_001191335.1:n.117-10135G=
ENST00000617770.4:c.117-10135G= ENSP00000479870.1:n.117-10135G=