Canonical Allele Identifier: CA2246104941
Gene: ALOX12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086216C= , CM000679.2:g.8086216C= GRCh38
NC_000017.10:g.7989534C= , CM000679.1:g.7989534C= GRCh37
NC_000017.9:g.7930259C= NCBI36
NG_007099.1:g.6488G=
NG_007099.2:g.6501G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.152G= MANE Select ENSP00000497784.1:p.Gly51=
ENST00000319144.4:c.152G= ENSP00000315167.4:p.Gly51=
NM_001139.2:c.152G= NP_001130.1:p.Gly51=
NM_001139.3:c.152G= MANE Select NP_001130.1:p.Gly51=