Canonical Allele Identifier: CA397989929
Gene: ALOX12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075677G>C , CM000679.2:g.8075677G>C GRCh38
NC_000017.10:g.7978995G>C , CM000679.1:g.7978995G>C GRCh37
NC_000017.9:g.7919720G>C NCBI36
NG_007099.1:g.17027C>G
NG_007099.2:g.17040C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1572C>G MANE Select ENSP00000497784.1:p.Asp524Glu
ENST00000649809.1:c.636C>G ENSP00000496845.1:p.Asp212Glu
ENST00000319144.4:c.1572C>G ENSP00000315167.4:p.Asp524Glu
ENST00000577351.5:n.479+498C>G
NM_001139.2:c.1572C>G NP_001130.1:p.Asp524Glu
NM_001139.3:c.1572C>G MANE Select NP_001130.1:p.Asp524Glu