Canonical Allele Identifier: CA2246104972

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8086241G= , CM000679.2:g.8086241G=	GRCh38
NC_000017.10:g.7989559G= , CM000679.1:g.7989559G=	GRCh37
NC_000017.9:g.7930284G=	NCBI36
NG_007099.1:g.6463C=
NG_007099.2:g.6476C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.148-21C= MANE Select	ENSP00000497784.1:n.148-21C=
ENST00000319144.4:c.148-21C=	ENSP00000315167.4:n.148-21C=
NM_001139.2:c.148-21C=	NP_001130.1:n.148-21C=
NM_001139.3:c.148-21C= MANE Select	NP_001130.1:n.148-21C=