Canonical Allele Identifier: CA397999513
Gene: ALOX12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086111T>A , CM000679.2:g.8086111T>A GRCh38
NC_000017.10:g.7989429T>A , CM000679.1:g.7989429T>A GRCh37
NC_000017.9:g.7930154T>A NCBI36
NG_007099.1:g.6593A>T
NG_007099.2:g.6606A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.257A>T MANE Select ENSP00000497784.1:p.Tyr86Phe
ENST00000319144.4:c.257A>T ENSP00000315167.4:p.Tyr86Phe
NM_001139.2:c.257A>T NP_001130.1:p.Tyr86Phe
NM_001139.3:c.257A>T MANE Select NP_001130.1:p.Tyr86Phe