Canonical Allele Identifier: CA397990935
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7979641C>G (hg19) chr17:g.8076323C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8076323C>G , CM000679.2:g.8076323C>G GRCh38
NC_000017.10:g.7979641C>G , CM000679.1:g.7979641C>G GRCh37
NC_000017.9:g.7920366C>G NCBI36
NG_007099.1:g.16381G>C
NG_007099.2:g.16394G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647874.1:c.1384G>C MANE Select ENSP00000497784.1:p.Gly462Arg
ENST00000649809.1:c.448G>C ENSP00000496845.1:p.Gly150Arg
ENST00000319144.4:c.1384G>C ENSP00000315167.4:p.Gly462Arg
ENST00000577351.5:n.331G>C
ENST00000583276.5:n.768G>C
ENST00000584116.1:n.640G>C
NM_001139.2:c.1384G>C NP_001130.1:p.Gly462Arg
NM_001139.3:c.1384G>C MANE Select NP_001130.1:p.Gly462Arg
Search 100 bp 5'
Search 100 bp 3'