Canonical Allele Identifier: CA397990058
Gene: ALOX12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075704C>G , CM000679.2:g.8075704C>G GRCh38
NC_000017.10:g.7979022C>G , CM000679.1:g.7979022C>G GRCh37
NC_000017.9:g.7919747C>G NCBI36
NG_007099.1:g.17000G>C
NG_007099.2:g.17013G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1545G>C MANE Select ENSP00000497784.1:p.Glu515Asp
ENST00000649809.1:c.609G>C ENSP00000496845.1:p.Glu203Asp
ENST00000319144.4:c.1545G>C ENSP00000315167.4:p.Glu515Asp
ENST00000577351.5:n.479+471G>C
NM_001139.2:c.1545G>C NP_001130.1:p.Glu515Asp
NM_001139.3:c.1545G>C MANE Select NP_001130.1:p.Glu515Asp