Canonical Allele Identifier: CA397999778
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7989460A>C (hg19) chr17:g.8086142A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086142A>C , CM000679.2:g.8086142A>C GRCh38
NC_000017.10:g.7989460A>C , CM000679.1:g.7989460A>C GRCh37
NC_000017.9:g.7930185A>C NCBI36
NG_007099.1:g.6562T>G
NG_007099.2:g.6575T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.226T>G MANE Select ENSP00000497784.1:p.Phe76Val
ENST00000319144.4:c.226T>G ENSP00000315167.4:p.Phe76Val
NM_001139.2:c.226T>G NP_001130.1:p.Phe76Val
NM_001139.3:c.226T>G MANE Select NP_001130.1:p.Phe76Val
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