Canonical Allele Identifier: CA2246125643

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8075659A= , CM000679.2:g.8075659A=	GRCh38
NC_000017.10:g.7978977A= , CM000679.1:g.7978977A=	GRCh37
NC_000017.9:g.7919702A=	NCBI36
NG_007099.1:g.17045T=
NG_007099.2:g.17058T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1590T= MANE Select	ENSP00000497784.1:p.Asp530=
ENST00000649809.1:c.654T=	ENSP00000496845.1:p.Asp218=
ENST00000319144.4:c.1590T=	ENSP00000315167.4:p.Asp530=
ENST00000577351.5:n.479+516T=
NM_001139.2:c.1590T=	NP_001130.1:p.Asp530=
NM_001139.3:c.1590T= MANE Select	NP_001130.1:p.Asp530=