Canonical Allele Identifier: CA2246126028
Gene: ALOX12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075856G= , CM000679.2:g.8075856G= GRCh38
NC_000017.10:g.7979174G= , CM000679.1:g.7979174G= GRCh37
NC_000017.9:g.7919899G= NCBI36
NG_007099.1:g.16848C=
NG_007099.2:g.16861C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1533-140C= MANE Select ENSP00000497784.1:n.1533-140C=
ENST00000649809.1:c.597-140C= ENSP00000496845.1:n.597-140C=
ENST00000319144.4:c.1533-140C= ENSP00000315167.4:n.1533-140C=
ENST00000577351.5:n.479+319C=
NM_001139.2:c.1533-140C= NP_001130.1:n.1533-140C=
NM_001139.3:c.1533-140C= MANE Select NP_001130.1:n.1533-140C=