Canonical Allele Identifier: CA2576161249

Gene: ALOX12B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8086280C>A , CM000679.2:g.8086280C>A	GRCh38
NC_000017.10:g.7989598C>A , CM000679.1:g.7989598C>A	GRCh37
NC_000017.9:g.7930323C>A	NCBI36
NG_007099.1:g.6424G>T
NG_007099.2:g.6437G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.148-60G>T MANE Select	ENSP00000497784.1:n.148-60G>T
ENST00000319144.4:c.148-60G>T	ENSP00000315167.4:n.148-60G>T
NM_001139.2:c.148-60G>T	NP_001130.1:n.148-60G>T
NM_001139.3:c.148-60G>T MANE Select	NP_001130.1:n.148-60G>T