Canonical Allele Identifier: CA497599087
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-6996990-G-T
MyVariant Identifiers: chr17:g.6900309G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996990G>T , CM000679.2:g.6996990G>T GRCh38
NC_000017.10:g.6900309G>T , CM000679.1:g.6900309G>T GRCh37
NC_000017.9:g.6841033G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.300G>T (ALOX12) MANE Select ENSP00000251535.6:p.Val100=
ENST00000251535.10:c.300G>T (ALOX12) ENSP00000251535.6:p.Val100=
ENST00000480801.1:c.9G>T (ALOX12) ENSP00000467033.1:p.Val3=
NM_000697.2:c.300G>T (ALOX12) NP_000688.2:p.Val100=
NR_040089.1:n.234-11450C>A (ALOX12-AS1)
XM_011523780.1:c.657G>T (ALOX12) XP_011522082.1:p.Val219=
XM_011523780.2:c.657G>T (ALOX12) XP_011522082.1:p.Val219=
NM_000697.3:c.300G>T (ALOX12) MANE Select NP_000688.2:p.Val100=
Search 100 bp 5'
Search 100 bp 3'