Canonical Allele Identifier: CA14370242
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1277668
ClinVar RCV Id: RCV001692825
dbSNP Id: rs2292350
gnomAD v2: 17-6901672-G-A
gnomAD v3: 17-6998353-G-A
gnomAD v4: 17-6998353-G-A
MyVariant Identifiers: chr17:g.6901672G>A (hg19) chr17:g.6998353G>A (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6998353G>A , CM000679.2:g.6998353G>A GRCh38
NC_000017.10:g.6901672G>A , CM000679.1:g.6901672G>A GRCh37
NC_000017.9:g.6842396G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000251535.11:c.338-156G>A (ALOX12) MANE Select ENSP00000251535.6:n.338-156G>A
ENST00000251535.10:c.338-156G>A (ALOX12) ENSP00000251535.6:n.338-156G>A
ENST00000480801.1:c.47-156G>A (ALOX12) ENSP00000467033.1:n.47-156G>A
NM_000697.2:c.338-156G>A (ALOX12) NP_000688.2:n.338-156G>A
NR_040089.1:n.233+11443C>T (ALOX12-AS1)
XM_011523780.1:c.695-156G>A (ALOX12) XP_011522082.1:n.695-156G>A
XM_011523780.2:c.695-156G>A (ALOX12) XP_011522082.1:n.695-156G>A
NM_000697.3:c.338-156G>A (ALOX12) MANE Select NP_000688.2:n.338-156G>A
Search 100 bp 5'
Search 100 bp 3'