Canonical Allele Identifier: CA397990056
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7979022C>A (hg19) chr17:g.8075704C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075704C>A , CM000679.2:g.8075704C>A GRCh38
NC_000017.10:g.7979022C>A , CM000679.1:g.7979022C>A GRCh37
NC_000017.9:g.7919747C>A NCBI36
NG_007099.1:g.17000G>T
NG_007099.2:g.17013G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647874.1:c.1545G>T MANE Select ENSP00000497784.1:p.Glu515Asp
ENST00000649809.1:c.609G>T ENSP00000496845.1:p.Glu203Asp
ENST00000319144.4:c.1545G>T ENSP00000315167.4:p.Glu515Asp
ENST00000577351.5:n.479+471G>T
NM_001139.2:c.1545G>T NP_001130.1:p.Glu515Asp
NM_001139.3:c.1545G>T MANE Select NP_001130.1:p.Glu515Asp
Search 100 bp 5'
Search 100 bp 3'