Canonical Allele Identifier: CA2246125607

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8075650C= , CM000679.2:g.8075650C=	GRCh38
NC_000017.10:g.7978968C= , CM000679.1:g.7978968C=	GRCh37
NC_000017.9:g.7919693C=	NCBI36
NG_007099.1:g.17054G=
NG_007099.2:g.17067G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1599G= MANE Select	ENSP00000497784.1:p.Leu533=
ENST00000649809.1:c.663G=	ENSP00000496845.1:p.Leu221=
ENST00000319144.4:c.1599G=	ENSP00000315167.4:p.Leu533=
ENST00000577351.5:n.479+525G=
NM_001139.2:c.1599G=	NP_001130.1:p.Leu533=
NM_001139.3:c.1599G= MANE Select	NP_001130.1:p.Leu533=