Canonical Allele Identifier: CA2246104816
Gene: ALOX12B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086166_8086169delinsGGAT , CM000679.2:g.8086166_8086169delinsGGAT GRCh38
NC_000017.10:g.7989484_7989487delinsGGAT , CM000679.1:g.7989484_7989487delinsGGAT GRCh37
NC_000017.9:g.7930209_7930212delinsGGAT NCBI36
NG_007099.1:g.6535_6538delinsATCC
NG_007099.2:g.6548_6551delinsATCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.199_202delinsATCC MANE Select ENSP00000497784.1:p.Ile67=
ENST00000319144.4:c.199_202delinsATCC ENSP00000315167.4:p.Ile67=
NM_001139.2:c.199_202delinsATCC NP_001130.1:p.Ile67=
NM_001139.3:c.199_202delinsATCC MANE Select NP_001130.1:p.Ile67=
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