Canonical Allele Identifier: CA2635961392
Gene: ALOX12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8085920dup , CM000679.2:g.8085920dup GRCh38
NC_000017.10:g.7989238dup , CM000679.1:g.7989238dup GRCh37
NC_000017.9:g.7929963dup NCBI36
NG_007099.1:g.6789dup
NG_007099.2:g.6802dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.352+101dup MANE Select ENSP00000497784.1:n.352+101dup
ENST00000319144.4:c.352+101dup ENSP00000315167.4:n.352+101dup
NM_001139.2:c.352+101dup NP_001130.1:n.352+101dup
NM_001139.3:c.352+101dup MANE Select NP_001130.1:n.352+101dup