Canonical Allele Identifier: CA397989862
Gene: ALOX12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075661C>A , CM000679.2:g.8075661C>A GRCh38
NC_000017.10:g.7978979C>A , CM000679.1:g.7978979C>A GRCh37
NC_000017.9:g.7919704C>A NCBI36
NG_007099.1:g.17043G>T
NG_007099.2:g.17056G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1588G>T MANE Select ENSP00000497784.1:p.Asp530Tyr
ENST00000649809.1:c.652G>T ENSP00000496845.1:p.Asp218Tyr
ENST00000319144.4:c.1588G>T ENSP00000315167.4:p.Asp530Tyr
ENST00000577351.5:n.479+514G>T
NM_001139.2:c.1588G>T NP_001130.1:p.Asp530Tyr
NM_001139.3:c.1588G>T MANE Select NP_001130.1:p.Asp530Tyr