Canonical Allele Identifier: CA397998885
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7989348A>T (hg19) chr17:g.8086030A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086030A>T , CM000679.2:g.8086030A>T GRCh38
NC_000017.10:g.7989348A>T , CM000679.1:g.7989348A>T GRCh37
NC_000017.9:g.7930073A>T NCBI36
NG_007099.1:g.6674T>A
NG_007099.2:g.6687T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.338T>A MANE Select ENSP00000497784.1:p.Leu113His
ENST00000319144.4:c.338T>A ENSP00000315167.4:p.Leu113His
NM_001139.2:c.338T>A NP_001130.1:p.Leu113His
NM_001139.3:c.338T>A MANE Select NP_001130.1:p.Leu113His
Search 100 bp 5'
Search 100 bp 3'