Canonical Allele Identifier: CA14370239
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1220801
ClinVar RCV Id: RCV001595363
dbSNP Id: rs2073438
gnomAD v2: 17-6900076-G-A
gnomAD v3: 17-6996757-G-A
gnomAD v4: 17-6996757-G-A

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