Canonical Allele Identifier: CA397999480
Gene: ALOX12B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086108A>C , CM000679.2:g.8086108A>C GRCh38
NC_000017.10:g.7989426A>C , CM000679.1:g.7989426A>C GRCh37
NC_000017.9:g.7930151A>C NCBI36
NG_007099.1:g.6596T>G
NG_007099.2:g.6609T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.260T>G MANE Select ENSP00000497784.1:p.Val87Gly
ENST00000319144.4:c.260T>G ENSP00000315167.4:p.Val87Gly
NM_001139.2:c.260T>G NP_001130.1:p.Val87Gly
NM_001139.3:c.260T>G MANE Select NP_001130.1:p.Val87Gly