Canonical Allele Identifier: CA2246104947
Gene: ALOX12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086217C= , CM000679.2:g.8086217C= GRCh38
NC_000017.10:g.7989535C= , CM000679.1:g.7989535C= GRCh37
NC_000017.9:g.7930260C= NCBI36
NG_007099.1:g.6487G=
NG_007099.2:g.6500G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.151G= MANE Select ENSP00000497784.1:p.Gly51=
ENST00000319144.4:c.151G= ENSP00000315167.4:p.Gly51=
NM_001139.2:c.151G= NP_001130.1:p.Gly51=
NM_001139.3:c.151G= MANE Select NP_001130.1:p.Gly51=