Canonical Allele Identifier: CA2246126463
Gene: ALOX12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076330G= , CM000679.2:g.8076330G= GRCh38
NC_000017.10:g.7979648G= , CM000679.1:g.7979648G= GRCh37
NC_000017.9:g.7920373G= NCBI36
NG_007099.1:g.16374C=
NG_007099.2:g.16387C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647874.1:c.1377C= MANE Select ENSP00000497784.1:p.Gly459=
ENST00000649809.1:c.441C= ENSP00000496845.1:p.Gly147=
ENST00000319144.4:c.1377C= ENSP00000315167.4:p.Gly459=
ENST00000577351.5:n.324C=
ENST00000583276.5:n.761C=
ENST00000584116.1:n.633C=
NM_001139.2:c.1377C= NP_001130.1:p.Gly459=
NM_001139.3:c.1377C= MANE Select NP_001130.1:p.Gly459=