Canonical Allele Identifier: CA397990065
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7979024C>A (hg19) chr17:g.8075706C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8075706C>A , CM000679.2:g.8075706C>A GRCh38
NC_000017.10:g.7979024C>A , CM000679.1:g.7979024C>A GRCh37
NC_000017.9:g.7919749C>A NCBI36
NG_007099.1:g.16998G>T
NG_007099.2:g.17011G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1543G>T MANE Select ENSP00000497784.1:p.Glu515Ter
ENST00000649809.1:c.607G>T ENSP00000496845.1:p.Glu203Ter
ENST00000319144.4:c.1543G>T ENSP00000315167.4:p.Glu515Ter
ENST00000577351.5:n.479+469G>T
NM_001139.2:c.1543G>T NP_001130.1:p.Glu515Ter
NM_001139.3:c.1543G>T MANE Select NP_001130.1:p.Glu515Ter
Search 100 bp 5'
Search 100 bp 3'