Canonical Allele Identifier: CA397738397
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs995628050
gnomAD v2: 17-6900344-C-T
gnomAD v4: 17-6997025-C-T
MyVariant Identifiers: chr17:g.6900344C>T (hg19) chr17:g.6997025C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6997025C>T , CM000679.2:g.6997025C>T GRCh38
NC_000017.10:g.6900344C>T , CM000679.1:g.6900344C>T GRCh37
NC_000017.9:g.6841068C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.335C>T (ALOX12) MANE Select ENSP00000251535.6:p.Thr112Ile
ENST00000251535.10:c.335C>T (ALOX12) ENSP00000251535.6:p.Thr112Ile
ENST00000480801.1:c.44C>T (ALOX12) ENSP00000467033.1:p.Thr15Ile
NM_000697.2:c.335C>T (ALOX12) NP_000688.2:p.Thr112Ile
NR_040089.1:n.234-11485G>A (ALOX12-AS1)
XM_011523780.1:c.692C>T (ALOX12) XP_011522082.1:p.Thr231Ile
XM_011523780.2:c.692C>T (ALOX12) XP_011522082.1:p.Thr231Ile
NM_000697.3:c.335C>T (ALOX12) MANE Select NP_000688.2:p.Thr112Ile
Search 100 bp 5'
Search 100 bp 3'