Canonical Allele Identifier: CA397738111
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-6996982-C-G
MyVariant Identifiers: chr17:g.6900301C>G (hg19) chr17:g.6996982C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996982C>G , CM000679.2:g.6996982C>G GRCh38
NC_000017.10:g.6900301C>G , CM000679.1:g.6900301C>G GRCh37
NC_000017.9:g.6841025C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.292C>G (ALOX12) MANE Select ENSP00000251535.6:p.Arg98Gly
ENST00000251535.10:c.292C>G (ALOX12) ENSP00000251535.6:p.Arg98Gly
ENST00000480801.1:c.1C>G (ALOX12) ENSP00000467033.1:p.Arg1Gly
NM_000697.2:c.292C>G (ALOX12) NP_000688.2:p.Arg98Gly
NR_040089.1:n.234-11442G>C (ALOX12-AS1)
XM_011523780.1:c.649C>G (ALOX12) XP_011522082.1:p.Arg217Gly
XM_011523780.2:c.649C>G (ALOX12) XP_011522082.1:p.Arg217Gly
NM_000697.3:c.292C>G (ALOX12) MANE Select NP_000688.2:p.Arg98Gly
Search 100 bp 5'
Search 100 bp 3'