Canonical Allele Identifier: CA497600739
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6905109A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001790A>C , CM000679.2:g.7001790A>C GRCh38
NC_000017.10:g.6905109A>C , CM000679.1:g.6905109A>C GRCh37
NC_000017.9:g.6845833A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1140A>C (ALOX12) MANE Select ENSP00000251535.6:p.Pro380=
ENST00000251535.10:c.1140A>C (ALOX12) ENSP00000251535.6:p.Pro380=
NM_000697.2:c.1140A>C (ALOX12) NP_000688.2:p.Pro380=
NR_040089.1:n.233+8006T>G (ALOX12-AS1)
XM_011523780.1:c.1290A>C (ALOX12) XP_011522082.1:p.Pro430=
XM_011523780.2:c.1290A>C (ALOX12) XP_011522082.1:p.Pro430=
NM_000697.3:c.1140A>C (ALOX12) MANE Select NP_000688.2:p.Pro380=
Search 100 bp 5'
Search 100 bp 3'