Canonical Allele Identifier: CA397999534
Gene: ALOX12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086112A>T , CM000679.2:g.8086112A>T GRCh38
NC_000017.10:g.7989430A>T , CM000679.1:g.7989430A>T GRCh37
NC_000017.9:g.7930155A>T NCBI36
NG_007099.1:g.6592T>A
NG_007099.2:g.6605T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.256T>A MANE Select ENSP00000497784.1:p.Tyr86Asn
ENST00000319144.4:c.256T>A ENSP00000315167.4:p.Tyr86Asn
NM_001139.2:c.256T>A NP_001130.1:p.Tyr86Asn
NM_001139.3:c.256T>A MANE Select NP_001130.1:p.Tyr86Asn