Canonical Allele Identifier: CA497759450
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7979648G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076330G>T , CM000679.2:g.8076330G>T GRCh38
NC_000017.10:g.7979648G>T , CM000679.1:g.7979648G>T GRCh37
NC_000017.9:g.7920373G>T NCBI36
NG_007099.1:g.16374C>A
NG_007099.2:g.16387C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1377C>A MANE Select ENSP00000497784.1:p.Gly459=
ENST00000649809.1:c.441C>A ENSP00000496845.1:p.Gly147=
ENST00000319144.4:c.1377C>A ENSP00000315167.4:p.Gly459=
ENST00000577351.5:n.324C>A
ENST00000583276.5:n.761C>A
ENST00000584116.1:n.633C>A
NM_001139.2:c.1377C>A NP_001130.1:p.Gly459=
NM_001139.3:c.1377C>A MANE Select NP_001130.1:p.Gly459=
Search 100 bp 5'
Search 100 bp 3'