Canonical Allele Identifier: CA8333399
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs764359028
ExAC: 17:6905035 G / A
gnomAD v2: 17-6905035-G-A
gnomAD v4: 17-7001716-G-A
MyVariant Identifiers: chr17:g.6905035G>A (hg19) chr17:g.7001716G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001716G>A , CM000679.2:g.7001716G>A GRCh38
NC_000017.10:g.6905035G>A , CM000679.1:g.6905035G>A GRCh37
NC_000017.9:g.6845759G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1066G>A (ALOX12) MANE Select ENSP00000251535.6:p.Glu356Lys
ENST00000251535.10:c.1066G>A (ALOX12) ENSP00000251535.6:p.Glu356Lys
NM_000697.2:c.1066G>A (ALOX12) NP_000688.2:p.Glu356Lys
NR_040089.1:n.233+8080C>T (ALOX12-AS1)
XM_011523780.1:c.1216G>A (ALOX12) XP_011522082.1:p.Glu406Lys
XM_011523780.2:c.1216G>A (ALOX12) XP_011522082.1:p.Glu406Lys
NM_000697.3:c.1066G>A (ALOX12) MANE Select NP_000688.2:p.Glu356Lys
Search 100 bp 5'
Search 100 bp 3'