Canonical Allele Identifier: CA2246105060

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8086295T= , CM000679.2:g.8086295T=	GRCh38
NC_000017.10:g.7989613T= , CM000679.1:g.7989613T=	GRCh37
NC_000017.9:g.7930338T=	NCBI36
NG_007099.1:g.6409A=
NG_007099.2:g.6422A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.148-75A= MANE Select	ENSP00000497784.1:n.148-75A=
ENST00000319144.4:c.148-75A=	ENSP00000315167.4:n.148-75A=
NM_001139.2:c.148-75A=	NP_001130.1:n.148-75A=
NM_001139.3:c.148-75A= MANE Select	NP_001130.1:n.148-75A=