Canonical Allele Identifier: CA397737471
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-6996878-T-A
MyVariant Identifiers: chr17:g.6900197T>A (hg19) chr17:g.6996878T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996878T>A , CM000679.2:g.6996878T>A GRCh38
NC_000017.10:g.6900197T>A , CM000679.1:g.6900197T>A GRCh37
NC_000017.9:g.6840921T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.188T>A (ALOX12) MANE Select ENSP00000251535.6:p.Val63Glu
ENST00000251535.10:c.188T>A (ALOX12) ENSP00000251535.6:p.Val63Glu
NM_000697.2:c.188T>A (ALOX12) NP_000688.2:p.Val63Glu
NR_040089.1:n.234-11338A>T (ALOX12-AS1)
XM_011523780.1:c.545T>A (ALOX12) XP_011522082.1:p.Val182Glu
XM_011523780.2:c.545T>A (ALOX12) XP_011522082.1:p.Val182Glu
NM_000697.3:c.188T>A (ALOX12) MANE Select NP_000688.2:p.Val63Glu
Search 100 bp 5'
Search 100 bp 3'