Canonical Allele Identifier: CA981238154
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs1978294659

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8085679dup , CM000679.2:g.8085679dup GRCh38
NC_000017.10:g.7988997dup , CM000679.1:g.7988997dup GRCh37
NC_000017.9:g.7929722dup NCBI36
NG_007099.1:g.7028dup
NG_007099.2:g.7041dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.352+340dup MANE Select ENSP00000497784.1:n.352+340dup
ENST00000319144.4:c.352+340dup ENSP00000315167.4:n.352+340dup
NM_001139.2:c.352+340dup NP_001130.1:n.352+340dup
NM_001139.3:c.352+340dup MANE Select NP_001130.1:n.352+340dup