Canonical Allele Identifier: CA8333398
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs113417479
ExAC: 17:6905034 C / A
gnomAD v2: 17-6905034-C-A
gnomAD v3: 17-7001715-C-A
gnomAD v4: 17-7001715-C-A
MyVariant Identifiers: chr17:g.6905034C>A (hg19) chr17:g.7001715C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001715C>A , CM000679.2:g.7001715C>A GRCh38
NC_000017.10:g.6905034C>A , CM000679.1:g.6905034C>A GRCh37
NC_000017.9:g.6845758C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1065C>A (ALOX12) MANE Select ENSP00000251535.6:p.His355Gln
ENST00000251535.10:c.1065C>A (ALOX12) ENSP00000251535.6:p.His355Gln
NM_000697.2:c.1065C>A (ALOX12) NP_000688.2:p.His355Gln
NR_040089.1:n.233+8081G>T (ALOX12-AS1)
XM_011523780.1:c.1215C>A (ALOX12) XP_011522082.1:p.His405Gln
XM_011523780.2:c.1215C>A (ALOX12) XP_011522082.1:p.His405Gln
NM_000697.3:c.1065C>A (ALOX12) MANE Select NP_000688.2:p.His355Gln
Search 100 bp 5'
Search 100 bp 3'