Canonical Allele Identifier: CA2246103929
Gene: ALOX12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8085733G= , CM000679.2:g.8085733G= GRCh38
NC_000017.10:g.7989051G= , CM000679.1:g.7989051G= GRCh37
NC_000017.9:g.7929776G= NCBI36
NG_007099.1:g.6971C=
NG_007099.2:g.6984C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.352+283C= MANE Select ENSP00000497784.1:n.352+283C=
ENST00000319144.4:c.352+283C= ENSP00000315167.4:n.352+283C=
NM_001139.2:c.352+283C= NP_001130.1:n.352+283C=
NM_001139.3:c.352+283C= MANE Select NP_001130.1:n.352+283C=