Canonical Allele Identifier: CA497600599
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-7001631-C-T
MyVariant Identifiers: chr17:g.6904950C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001631C>T , CM000679.2:g.7001631C>T GRCh38
NC_000017.10:g.6904950C>T , CM000679.1:g.6904950C>T GRCh37
NC_000017.9:g.6845674C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.981C>T (ALOX12) MANE Select ENSP00000251535.6:p.Thr327=
ENST00000251535.10:c.981C>T (ALOX12) ENSP00000251535.6:p.Thr327=
NM_000697.2:c.981C>T (ALOX12) NP_000688.2:p.Thr327=
NR_040089.1:n.233+8165G>A (ALOX12-AS1)
XM_011523780.1:c.1131C>T (ALOX12) XP_011522082.1:p.Thr377=
XM_011523780.2:c.1131C>T (ALOX12) XP_011522082.1:p.Thr377=
NM_000697.3:c.981C>T (ALOX12) MANE Select NP_000688.2:p.Thr327=
Search 100 bp 5'
Search 100 bp 3'