Canonical Allele Identifier: CA2246125250
Gene: ALOX12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075471T= , CM000679.2:g.8075471T= GRCh38
NC_000017.10:g.7978789T= , CM000679.1:g.7978789T= GRCh37
NC_000017.9:g.7919514T= NCBI36
NG_007099.1:g.17233A=
NG_007099.2:g.17246A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1654+124A= MANE Select ENSP00000497784.1:n.1654+124A=
ENST00000649809.1:c.718+124A= ENSP00000496845.1:n.718+124A=
ENST00000319144.4:c.1654+124A= ENSP00000315167.4:n.1654+124A=
ENST00000577351.5:n.479+704A=
NM_001139.2:c.1654+124A= NP_001130.1:n.1654+124A=
NM_001139.3:c.1654+124A= MANE Select NP_001130.1:n.1654+124A=