Canonical Allele Identifier: CA397737408
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-6996866-T-C
MyVariant Identifiers: chr17:g.6900185T>C (hg19) chr17:g.6996866T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996866T>C , CM000679.2:g.6996866T>C GRCh38
NC_000017.10:g.6900185T>C , CM000679.1:g.6900185T>C GRCh37
NC_000017.9:g.6840909T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.176T>C (ALOX12) MANE Select ENSP00000251535.6:p.Leu59Pro
ENST00000251535.10:c.176T>C (ALOX12) ENSP00000251535.6:p.Leu59Pro
NM_000697.2:c.176T>C (ALOX12) NP_000688.2:p.Leu59Pro
NR_040089.1:n.234-11326A>G (ALOX12-AS1)
XM_011523780.1:c.533T>C (ALOX12) XP_011522082.1:p.Leu178Pro
XM_011523780.2:c.533T>C (ALOX12) XP_011522082.1:p.Leu178Pro
NM_000697.3:c.176T>C (ALOX12) MANE Select NP_000688.2:p.Leu59Pro
Search 100 bp 5'
Search 100 bp 3'