Canonical Allele Identifier: CA2246104990

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8086261C= , CM000679.2:g.8086261C=	GRCh38
NC_000017.10:g.7989579C= , CM000679.1:g.7989579C=	GRCh37
NC_000017.9:g.7930304C=	NCBI36
NG_007099.1:g.6443G=
NG_007099.2:g.6456G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.148-41G= MANE Select	ENSP00000497784.1:n.148-41G=
ENST00000319144.4:c.148-41G=	ENSP00000315167.4:n.148-41G=
NM_001139.2:c.148-41G=	NP_001130.1:n.148-41G=
NM_001139.3:c.148-41G= MANE Select	NP_001130.1:n.148-41G=