Canonical Allele Identifier: CA14370240
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1262015
ClinVar RCV Id: RCV001667134
dbSNP Id: rs2070590
gnomAD v2: 17-6900444-T-G
gnomAD v3: 17-6997125-T-G
gnomAD v4: 17-6997125-T-G
MyVariant Identifiers: chr17:g.6900444T>G (hg19) chr17:g.6997125T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6997125T>G , CM000679.2:g.6997125T>G GRCh38
NC_000017.10:g.6900444T>G , CM000679.1:g.6900444T>G GRCh37
NC_000017.9:g.6841168T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.337+98T>G (ALOX12) MANE Select ENSP00000251535.6:n.337+98T>G
ENST00000251535.10:c.337+98T>G (ALOX12) ENSP00000251535.6:n.337+98T>G
ENST00000480801.1:c.46+98T>G (ALOX12) ENSP00000467033.1:n.46+98T>G
NM_000697.2:c.337+98T>G (ALOX12) NP_000688.2:n.337+98T>G
NR_040089.1:n.234-11585A>C (ALOX12-AS1)
XM_011523780.1:c.694+98T>G (ALOX12) XP_011522082.1:n.694+98T>G
XM_011523780.2:c.694+98T>G (ALOX12) XP_011522082.1:n.694+98T>G
NM_000697.3:c.337+98T>G (ALOX12) MANE Select NP_000688.2:n.337+98T>G
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