Canonical Allele Identifier: CA2246126413

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8076273G= , CM000679.2:g.8076273G=	GRCh38
NC_000017.10:g.7979591G= , CM000679.1:g.7979591G=	GRCh37
NC_000017.9:g.7920316G=	NCBI36
NG_007099.1:g.16431C=
NG_007099.2:g.16444C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1434C= MANE Select	ENSP00000497784.1:p.Ser478=
ENST00000649809.1:c.498C=	ENSP00000496845.1:p.Ser166=
ENST00000319144.4:c.1434C=	ENSP00000315167.4:p.Ser478=
ENST00000577351.5:n.381C=
ENST00000583276.5:n.818C=
NM_001139.2:c.1434C=	NP_001130.1:p.Ser478=
NM_001139.3:c.1434C= MANE Select	NP_001130.1:p.Ser478=