Canonical Allele Identifier: CA397999910
Gene: ALOX12B HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.7989484G>C (hg19) chr17:g.8086166G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086166G>C , CM000679.2:g.8086166G>C GRCh38
NC_000017.10:g.7989484G>C , CM000679.1:g.7989484G>C GRCh37
NC_000017.9:g.7930209G>C NCBI36
NG_007099.1:g.6538C>G
NG_007099.2:g.6551C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.202C>G MANE Select ENSP00000497784.1:p.Arg68Gly
ENST00000319144.4:c.202C>G ENSP00000315167.4:p.Arg68Gly
NM_001139.2:c.202C>G NP_001130.1:p.Arg68Gly
NM_001139.3:c.202C>G MANE Select NP_001130.1:p.Arg68Gly
Search 100 bp 5'
Search 100 bp 3'