Canonical Allele Identifier: CA2576161245
Gene: ALOX12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086250del , CM000679.2:g.8086250del GRCh38
NC_000017.10:g.7989568del , CM000679.1:g.7989568del GRCh37
NC_000017.9:g.7930293del NCBI36
NG_007099.1:g.6456del
NG_007099.2:g.6469del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.148-28del MANE Select ENSP00000497784.1:n.148-28del
ENST00000319144.4:c.148-28del ENSP00000315167.4:n.148-28del
NM_001139.2:c.148-28del NP_001130.1:n.148-28del
NM_001139.3:c.148-28del MANE Select NP_001130.1:n.148-28del
Search 100 bp 5'
Search 100 bp 3'