Canonical Allele Identifier: CA2246125262
Gene: ALOX12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075496A= , CM000679.2:g.8075496A= GRCh38
NC_000017.10:g.7978814A= , CM000679.1:g.7978814A= GRCh37
NC_000017.9:g.7919539A= NCBI36
NG_007099.1:g.17208T=
NG_007099.2:g.17221T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1654+99T= MANE Select ENSP00000497784.1:n.1654+99T=
ENST00000649809.1:c.718+99T= ENSP00000496845.1:n.718+99T=
ENST00000319144.4:c.1654+99T= ENSP00000315167.4:n.1654+99T=
ENST00000577351.5:n.479+679T=
NM_001139.2:c.1654+99T= NP_001130.1:n.1654+99T=
NM_001139.3:c.1654+99T= MANE Select NP_001130.1:n.1654+99T=