Canonical Allele Identifier: CA2246125210

Gene: ALOX12B

Linked Data

• dbSNP Id: rs1977058388

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1654+165T>G MANE Select	ENSP00000497784.1:n.1654+165T>G
ENST00000649809.1:c.718+165T>G	ENSP00000496845.1:n.718+165T>G
ENST00000319144.4:c.1654+165T>G	ENSP00000315167.4:n.1654+165T>G
ENST00000577351.5:n.479+745T>G
NM_001139.2:c.1654+165T>G	NP_001130.1:n.1654+165T>G
NM_001139.3:c.1654+165T>G MANE Select	NP_001130.1:n.1654+165T>G