Canonical Allele Identifier: CA2246104565
Gene: ALOX12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086074G= , CM000679.2:g.8086074G= GRCh38
NC_000017.10:g.7989392G= , CM000679.1:g.7989392G= GRCh37
NC_000017.9:g.7930117G= NCBI36
NG_007099.1:g.6630C=
NG_007099.2:g.6643C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.294C= MANE Select ENSP00000497784.1:p.His98=
ENST00000319144.4:c.294C= ENSP00000315167.4:p.His98=
NM_001139.2:c.294C= NP_001130.1:p.His98=
NM_001139.3:c.294C= MANE Select NP_001130.1:p.His98=