Canonical Allele Identifier: CA397747866
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6904962C>A (hg19) chr17:g.7001643C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001643C>A , CM000679.2:g.7001643C>A GRCh38
NC_000017.10:g.6904962C>A , CM000679.1:g.6904962C>A GRCh37
NC_000017.9:g.6845686C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.993C>A (ALOX12) MANE Select ENSP00000251535.6:p.Phe331Leu
ENST00000251535.10:c.993C>A (ALOX12) ENSP00000251535.6:p.Phe331Leu
NM_000697.2:c.993C>A (ALOX12) NP_000688.2:p.Phe331Leu
NR_040089.1:n.233+8153G>T (ALOX12-AS1)
XM_011523780.1:c.1143C>A (ALOX12) XP_011522082.1:p.Phe381Leu
XM_011523780.2:c.1143C>A (ALOX12) XP_011522082.1:p.Phe381Leu
NM_000697.3:c.993C>A (ALOX12) MANE Select NP_000688.2:p.Phe331Leu
Search 100 bp 5'
Search 100 bp 3'