Canonical Allele Identifier: CA397738319
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1351796588
gnomAD v2: 17-6900330-C-A
gnomAD v4: 17-6997011-C-A
MyVariant Identifiers: chr17:g.6900330C>A (hg19) chr17:g.6997011C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6997011C>A , CM000679.2:g.6997011C>A GRCh38
NC_000017.10:g.6900330C>A , CM000679.1:g.6900330C>A GRCh37
NC_000017.9:g.6841054C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.321C>A (ALOX12) MANE Select ENSP00000251535.6:p.Ser107Arg
ENST00000251535.10:c.321C>A (ALOX12) ENSP00000251535.6:p.Ser107Arg
ENST00000480801.1:c.30C>A (ALOX12) ENSP00000467033.1:p.Ser10Arg
NM_000697.2:c.321C>A (ALOX12) NP_000688.2:p.Ser107Arg
NR_040089.1:n.234-11471G>T (ALOX12-AS1)
XM_011523780.1:c.678C>A (ALOX12) XP_011522082.1:p.Ser226Arg
XM_011523780.2:c.678C>A (ALOX12) XP_011522082.1:p.Ser226Arg
NM_000697.3:c.321C>A (ALOX12) MANE Select NP_000688.2:p.Ser107Arg
Search 100 bp 5'
Search 100 bp 3'