Canonical Allele Identifier: CA397737233
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1180104274
gnomAD v2: 17-6900154-T-A
gnomAD v4: 17-6996835-T-A
MyVariant Identifiers: chr17:g.6900154T>A (hg19) chr17:g.6996835T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996835T>A , CM000679.2:g.6996835T>A GRCh38
NC_000017.10:g.6900154T>A , CM000679.1:g.6900154T>A GRCh37
NC_000017.9:g.6840878T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.145T>A (ALOX12) MANE Select ENSP00000251535.6:p.Phe49Ile
ENST00000251535.10:c.145T>A (ALOX12) ENSP00000251535.6:p.Phe49Ile
NM_000697.2:c.145T>A (ALOX12) NP_000688.2:p.Phe49Ile
NR_040089.1:n.234-11295A>T (ALOX12-AS1)
XM_011523780.1:c.502T>A (ALOX12) XP_011522082.1:p.Phe168Ile
XM_011523780.2:c.502T>A (ALOX12) XP_011522082.1:p.Phe168Ile
NM_000697.3:c.145T>A (ALOX12) MANE Select NP_000688.2:p.Phe49Ile
Search 100 bp 5'
Search 100 bp 3'