Canonical Allele Identifier: CA397738353
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1402394653
gnomAD v3: 17-6997018-G-C
gnomAD v4: 17-6997018-G-C
MyVariant Identifiers: chr17:g.6900337G>C (hg19) chr17:g.6997018G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6997018G>C , CM000679.2:g.6997018G>C GRCh38
NC_000017.10:g.6900337G>C , CM000679.1:g.6900337G>C GRCh37
NC_000017.9:g.6841061G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.328G>C (ALOX12) MANE Select ENSP00000251535.6:p.Glu110Gln
ENST00000251535.10:c.328G>C (ALOX12) ENSP00000251535.6:p.Glu110Gln
ENST00000480801.1:c.37G>C (ALOX12) ENSP00000467033.1:p.Glu13Gln
NM_000697.2:c.328G>C (ALOX12) NP_000688.2:p.Glu110Gln
NR_040089.1:n.234-11478C>G (ALOX12-AS1)
XM_011523780.1:c.685G>C (ALOX12) XP_011522082.1:p.Glu229Gln
XM_011523780.2:c.685G>C (ALOX12) XP_011522082.1:p.Glu229Gln
NM_000697.3:c.328G>C (ALOX12) MANE Select NP_000688.2:p.Glu110Gln
Search 100 bp 5'
Search 100 bp 3'