Canonical Allele Identifier: CA2246103861
Gene: ALOX12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8085695C= , CM000679.2:g.8085695C= GRCh38
NC_000017.10:g.7989013C= , CM000679.1:g.7989013C= GRCh37
NC_000017.9:g.7929738C= NCBI36
NG_007099.1:g.7009G=
NG_007099.2:g.7022G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.352+321G= MANE Select ENSP00000497784.1:n.352+321G=
ENST00000319144.4:c.352+321G= ENSP00000315167.4:n.352+321G=
NM_001139.2:c.352+321G= NP_001130.1:n.352+321G=
NM_001139.3:c.352+321G= MANE Select NP_001130.1:n.352+321G=