Canonical Allele Identifier: CA397737423
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6900188T>G (hg19) chr17:g.6996869T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996869T>G , CM000679.2:g.6996869T>G GRCh38
NC_000017.10:g.6900188T>G , CM000679.1:g.6900188T>G GRCh37
NC_000017.9:g.6840912T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.179T>G (ALOX12) MANE Select ENSP00000251535.6:p.Leu60Arg
ENST00000251535.10:c.179T>G (ALOX12) ENSP00000251535.6:p.Leu60Arg
NM_000697.2:c.179T>G (ALOX12) NP_000688.2:p.Leu60Arg
NR_040089.1:n.234-11329A>C (ALOX12-AS1)
XM_011523780.1:c.536T>G (ALOX12) XP_011522082.1:p.Leu179Arg
XM_011523780.2:c.536T>G (ALOX12) XP_011522082.1:p.Leu179Arg
NM_000697.3:c.179T>G (ALOX12) MANE Select NP_000688.2:p.Leu60Arg
Search 100 bp 5'
Search 100 bp 3'