Canonical Allele Identifier: CA2246125209
Gene: ALOX12B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075430A= , CM000679.2:g.8075430A= GRCh38
NC_000017.10:g.7978748A= , CM000679.1:g.7978748A= GRCh37
NC_000017.9:g.7919473A= NCBI36
NG_007099.1:g.17274T=
NG_007099.2:g.17287T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1654+165T= MANE Select ENSP00000497784.1:n.1654+165T=
ENST00000649809.1:c.718+165T= ENSP00000496845.1:n.718+165T=
ENST00000319144.4:c.1654+165T= ENSP00000315167.4:n.1654+165T=
ENST00000577351.5:n.479+745T=
NM_001139.2:c.1654+165T= NP_001130.1:n.1654+165T=
NM_001139.3:c.1654+165T= MANE Select NP_001130.1:n.1654+165T=
Search 100 bp 5'
Search 100 bp 3'