Canonical Allele Identifier: CA397990948
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7979643T>C (hg19) chr17:g.8076325T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076325T>C , CM000679.2:g.8076325T>C GRCh38
NC_000017.10:g.7979643T>C , CM000679.1:g.7979643T>C GRCh37
NC_000017.9:g.7920368T>C NCBI36
NG_007099.1:g.16379A>G
NG_007099.2:g.16392A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.1382A>G MANE Select ENSP00000497784.1:p.Glu461Gly
ENST00000649809.1:c.446A>G ENSP00000496845.1:p.Glu149Gly
ENST00000319144.4:c.1382A>G ENSP00000315167.4:p.Glu461Gly
ENST00000577351.5:n.329A>G
ENST00000583276.5:n.766A>G
ENST00000584116.1:n.638A>G
NM_001139.2:c.1382A>G NP_001130.1:p.Glu461Gly
NM_001139.3:c.1382A>G MANE Select NP_001130.1:p.Glu461Gly
Search 100 bp 5'
Search 100 bp 3'