Canonical Allele Identifier: CA913191195
Gene: ALOX12B HGNC NCBI

Linked Data

ClinVar Variation Id: 633825
ClinVar RCV Id: RCV000782411
dbSNP Id: rs1567985261
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086082_8086083dup , CM000679.2:g.8086082_8086083dup GRCh38
NC_000017.10:g.7989400_7989401dup , CM000679.1:g.7989400_7989401dup GRCh37
NC_000017.9:g.7930125_7930126dup NCBI36
NG_007099.1:g.6622_6623dup
NG_007099.2:g.6635_6636dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.286_287dup MANE Select ENSP00000497784.1:p.Tyr97SerfsTer?
ENST00000319144.4:c.286_287dup ENSP00000315167.4:p.Tyr97SerfsTer?
NM_001139.2:c.286_287dup NP_001130.1:p.Tyr97SerfsTer?
NM_001139.3:c.286_287dup MANE Select NP_001130.1:p.Tyr97SerfsTer?
Search 100 bp 5'
Search 100 bp 3'