Canonical Allele Identifier: CA397749232
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6905125T>G (hg19) chr17:g.7001806T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001806T>G , CM000679.2:g.7001806T>G GRCh38
NC_000017.10:g.6905125T>G , CM000679.1:g.6905125T>G GRCh37
NC_000017.9:g.6845849T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1156T>G (ALOX12) MANE Select ENSP00000251535.6:p.Phe386Val
ENST00000251535.10:c.1156T>G (ALOX12) ENSP00000251535.6:p.Phe386Val
NM_000697.2:c.1156T>G (ALOX12) NP_000688.2:p.Phe386Val
NR_040089.1:n.233+7990A>C (ALOX12-AS1)
XM_011523780.1:c.1306T>G (ALOX12) XP_011522082.1:p.Phe436Val
XM_011523780.2:c.1306T>G (ALOX12) XP_011522082.1:p.Phe436Val
NM_000697.3:c.1156T>G (ALOX12) MANE Select NP_000688.2:p.Phe386Val
Search 100 bp 5'
Search 100 bp 3'