Canonical Allele Identifier: CA2246105093

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8086318C= , CM000679.2:g.8086318C=	GRCh38
NC_000017.10:g.7989636C= , CM000679.1:g.7989636C=	GRCh37
NC_000017.9:g.7930361C=	NCBI36
NG_007099.1:g.6386G=
NG_007099.2:g.6399G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.148-98G= MANE Select	ENSP00000497784.1:n.148-98G=
ENST00000319144.4:c.148-98G=	ENSP00000315167.4:n.148-98G=
NM_001139.2:c.148-98G=	NP_001130.1:n.148-98G=
NM_001139.3:c.148-98G= MANE Select	NP_001130.1:n.148-98G=