Canonical Allele Identifier: CA287375761
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs764270877
gnomAD v2: 17-6905308-A-G
gnomAD v3: 17-7001989-A-G
gnomAD v4: 17-7001989-A-G
MyVariant Identifiers: chr17:g.6905308A>G (hg19) chr17:g.7001989A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001989A>G , CM000679.2:g.7001989A>G GRCh38
NC_000017.10:g.6905308A>G , CM000679.1:g.6905308A>G GRCh37
NC_000017.9:g.6846032A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1161+178A>G (ALOX12) MANE Select ENSP00000251535.6:n.1161+178A>G
ENST00000251535.10:c.1161+178A>G (ALOX12) ENSP00000251535.6:n.1161+178A>G
NM_000697.2:c.1161+178A>G (ALOX12) NP_000688.2:n.1161+178A>G
NR_040089.1:n.233+7807T>C (ALOX12-AS1)
XM_011523780.1:c.1311+178A>G (ALOX12) XP_011522082.1:n.1311+178A>G
XM_011523780.2:c.1311+178A>G (ALOX12) XP_011522082.1:n.1311+178A>G
NM_000697.3:c.1161+178A>G (ALOX12) MANE Select NP_000688.2:n.1161+178A>G
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