Canonical Allele Identifier: CA2246104935
Gene: ALOX12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086211A= , CM000679.2:g.8086211A= GRCh38
NC_000017.10:g.7989529A= , CM000679.1:g.7989529A= GRCh37
NC_000017.9:g.7930254A= NCBI36
NG_007099.1:g.6493T=
NG_007099.2:g.6506T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.157T= MANE Select ENSP00000497784.1:p.Tyr53=
ENST00000319144.4:c.157T= ENSP00000315167.4:p.Tyr53=
NM_001139.2:c.157T= NP_001130.1:p.Tyr53=
NM_001139.3:c.157T= MANE Select NP_001130.1:p.Tyr53=