Canonical Allele Identifier: CA287378588
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs566755026
gnomAD v3: 17-7004933-T-G
gnomAD v4: 17-7004933-T-G
MyVariant Identifiers: chr17:g.6908252T>G (hg19) chr17:g.7004933T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7004933T>G , CM000679.2:g.7004933T>G GRCh38
NC_000017.10:g.6908252T>G , CM000679.1:g.6908252T>G GRCh37
NC_000017.9:g.6848976T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000251535.11:c.1162-324T>G (ALOX12) MANE Select ENSP00000251535.6:n.1162-324T>G
ENST00000251535.10:c.1162-324T>G (ALOX12) ENSP00000251535.6:n.1162-324T>G
NM_000697.2:c.1162-324T>G (ALOX12) NP_000688.2:n.1162-324T>G
NR_040089.1:n.233+4863A>C (ALOX12-AS1)
XM_011523780.1:c.1312-324T>G (ALOX12) XP_011522082.1:n.1312-324T>G
XM_011523780.2:c.1312-324T>G (ALOX12) XP_011522082.1:n.1312-324T>G
NM_000697.3:c.1162-324T>G (ALOX12) MANE Select NP_000688.2:n.1162-324T>G
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