Canonical Allele Identifier: CA14370239
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI
COSMIC:
COSN6660293 (not active)
COSN19656341 (not active)
MyVariant.info:
GRCh38 chr17:g.6996757G>A
GRCh37 chr17:g.6900076G>A
gnomAD v2:
17:6900076 G / A
gnomAD v3:
17:6996757 G / A
gnomAD v4:
chr17-6996757-G-A
Joint Max Group AF 0.29735702 (EAS)
Genomes Max Group AF 0.31283197 (EAS)
Exomes Max Group AF 0.29379648 (EAS)
ClinVar RCV:
RCV001595363
ClinVar Variation:
1220801
dbSNP:
2073438
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996757G>A , CM000679.2:g.6996757G>A GRCh38
NC_000017.10:g.6900076G>A , CM000679.1:g.6900076G>A GRCh37
NC_000017.9:g.6840800G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.136-69G>A (ALOX12) MANE Select ENSP00000251535.6:n.136-69G>A
ENST00000251535.10:c.136-69G>A (ALOX12) ENSP00000251535.6:n.136-69G>A
NM_000697.2:c.136-69G>A (ALOX12) NP_000688.2:n.136-69G>A
NR_040089.1:n.234-11217C>T (ALOX12-AS1)
XM_011523780.1:c.493-69G>A (ALOX12) XP_011522082.1:n.493-69G>A
XM_011523780.2:c.493-69G>A (ALOX12) XP_011522082.1:n.493-69G>A
NM_000697.3:c.136-69G>A (ALOX12) MANE Select NP_000688.2:n.136-69G>A
Search 100 bp 5'
Search 100 bp 3'