Canonical Allele Identifier: CA2246125745

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8075692A= , CM000679.2:g.8075692A=	GRCh38
NC_000017.10:g.7979010A= , CM000679.1:g.7979010A=	GRCh37
NC_000017.9:g.7919735A=	NCBI36
NG_007099.1:g.17012T=
NG_007099.2:g.17025T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1557T= MANE Select	ENSP00000497784.1:p.Tyr519=
ENST00000649809.1:c.621T=	ENSP00000496845.1:p.Tyr207=
ENST00000319144.4:c.1557T=	ENSP00000315167.4:p.Tyr519=
ENST00000577351.5:n.479+483T=
NM_001139.2:c.1557T=	NP_001130.1:p.Tyr519=
NM_001139.3:c.1557T= MANE Select	NP_001130.1:p.Tyr519=