Canonical Allele Identifier: CA2246125280
Gene: ALOX12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075503C= , CM000679.2:g.8075503C= GRCh38
NC_000017.10:g.7978821C= , CM000679.1:g.7978821C= GRCh37
NC_000017.9:g.7919546C= NCBI36
NG_007099.1:g.17201G=
NG_007099.2:g.17214G=

Transcript Alleles

HGVS Amino-acid change
ENST00000647874.1:c.1654+92G= MANE Select ENSP00000497784.1:n.1654+92G=
ENST00000649809.1:c.718+92G= ENSP00000496845.1:n.718+92G=
ENST00000319144.4:c.1654+92G= ENSP00000315167.4:n.1654+92G=
ENST00000577351.5:n.479+672G=
NM_001139.2:c.1654+92G= NP_001130.1:n.1654+92G=
NM_001139.3:c.1654+92G= MANE Select NP_001130.1:n.1654+92G=