Canonical Allele Identifier: CA397737957
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1291925434
gnomAD v2: 17-6900284-T-A
gnomAD v3: 17-6996965-T-A
gnomAD v4: 17-6996965-T-A
MyVariant Identifiers: chr17:g.6900284T>A (hg19) chr17:g.6996965T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996965T>A , CM000679.2:g.6996965T>A GRCh38
NC_000017.10:g.6900284T>A , CM000679.1:g.6900284T>A GRCh37
NC_000017.9:g.6841008T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.275T>A (ALOX12) MANE Select ENSP00000251535.6:p.Val92Glu
ENST00000251535.10:c.275T>A (ALOX12) ENSP00000251535.6:p.Val92Glu
NM_000697.2:c.275T>A (ALOX12) NP_000688.2:p.Val92Glu
NR_040089.1:n.234-11425A>T (ALOX12-AS1)
XM_011523780.1:c.632T>A (ALOX12) XP_011522082.1:p.Val211Glu
XM_011523780.2:c.632T>A (ALOX12) XP_011522082.1:p.Val211Glu
NM_000697.3:c.275T>A (ALOX12) MANE Select NP_000688.2:p.Val92Glu
Search 100 bp 5'
Search 100 bp 3'