Canonical Allele Identifier: CA2246126469
Gene: ALOX12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076333C= , CM000679.2:g.8076333C= GRCh38
NC_000017.10:g.7979651C= , CM000679.1:g.7979651C= GRCh37
NC_000017.9:g.7920376C= NCBI36
NG_007099.1:g.16371G=
NG_007099.2:g.16384G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647874.1:c.1374G= MANE Select ENSP00000497784.1:p.Leu458=
ENST00000649809.1:c.438G= ENSP00000496845.1:p.Leu146=
ENST00000319144.4:c.1374G= ENSP00000315167.4:p.Leu458=
ENST00000577351.5:n.321G=
ENST00000583276.5:n.758G=
ENST00000584116.1:n.630G=
NM_001139.2:c.1374G= NP_001130.1:p.Leu458=
NM_001139.3:c.1374G= MANE Select NP_001130.1:p.Leu458=