Canonical Allele Identifier: CA397999707
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7989449C>G (hg19) chr17:g.8086131C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086131C>G , CM000679.2:g.8086131C>G GRCh38
NC_000017.10:g.7989449C>G , CM000679.1:g.7989449C>G GRCh37
NC_000017.9:g.7930174C>G NCBI36
NG_007099.1:g.6573G>C
NG_007099.2:g.6586G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.237G>C MANE Select ENSP00000497784.1:p.Lys79Asn
ENST00000319144.4:c.237G>C ENSP00000315167.4:p.Lys79Asn
NM_001139.2:c.237G>C NP_001130.1:p.Lys79Asn
NM_001139.3:c.237G>C MANE Select NP_001130.1:p.Lys79Asn
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