Canonical Allele Identifier: CA398000129
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7989525G>T (hg19) chr17:g.8086207G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086207G>T , CM000679.2:g.8086207G>T GRCh38
NC_000017.10:g.7989525G>T , CM000679.1:g.7989525G>T GRCh37
NC_000017.9:g.7930250G>T NCBI36
NG_007099.1:g.6497C>A
NG_007099.2:g.6510C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.161C>A MANE Select ENSP00000497784.1:p.Thr54Asn
ENST00000319144.4:c.161C>A ENSP00000315167.4:p.Thr54Asn
NM_001139.2:c.161C>A NP_001130.1:p.Thr54Asn
NM_001139.3:c.161C>A MANE Select NP_001130.1:p.Thr54Asn
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