Canonical Allele Identifier: CA2246125772
Gene: ALOX12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075701G= , CM000679.2:g.8075701G= GRCh38
NC_000017.10:g.7979019G= , CM000679.1:g.7979019G= GRCh37
NC_000017.9:g.7919744G= NCBI36
NG_007099.1:g.17003C=
NG_007099.2:g.17016C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647874.1:c.1548C= MANE Select ENSP00000497784.1:p.Ile516=
ENST00000649809.1:c.612C= ENSP00000496845.1:p.Ile204=
ENST00000319144.4:c.1548C= ENSP00000315167.4:p.Ile516=
ENST00000577351.5:n.479+474C=
NM_001139.2:c.1548C= NP_001130.1:p.Ile516=
NM_001139.3:c.1548C= MANE Select NP_001130.1:p.Ile516=