Canonical Allele Identifier: CA2832570355

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8075786T>A , CM000679.2:g.8075786T>A	GRCh38
NC_000017.10:g.7979104T>A , CM000679.1:g.7979104T>A	GRCh37
NC_000017.9:g.7919829T>A	NCBI36
NG_007099.1:g.16918A>T
NG_007099.2:g.16931A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1533-70A>T MANE Select	ENSP00000497784.1:n.1533-70A>T
ENST00000649809.1:c.597-70A>T	ENSP00000496845.1:n.597-70A>T
ENST00000319144.4:c.1533-70A>T	ENSP00000315167.4:n.1533-70A>T
ENST00000577351.5:n.479+389A>T
NM_001139.2:c.1533-70A>T	NP_001130.1:n.1533-70A>T
NM_001139.3:c.1533-70A>T MANE Select	NP_001130.1:n.1533-70A>T