Canonical Allele Identifier: CA2245576203
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1908732410

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001912T>C , CM000679.2:g.7001912T>C GRCh38
NC_000017.10:g.6905231T>C , CM000679.1:g.6905231T>C GRCh37
NC_000017.9:g.6845955T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1161+101T>C (ALOX12) MANE Select ENSP00000251535.6:n.1161+101T>C
ENST00000251535.10:c.1161+101T>C (ALOX12) ENSP00000251535.6:n.1161+101T>C
NM_000697.2:c.1161+101T>C (ALOX12) NP_000688.2:n.1161+101T>C
NR_040089.1:n.233+7884A>G (ALOX12-AS1)
XM_011523780.1:c.1311+101T>C (ALOX12) XP_011522082.1:n.1311+101T>C
XM_011523780.2:c.1311+101T>C (ALOX12) XP_011522082.1:n.1311+101T>C
NM_000697.3:c.1161+101T>C (ALOX12) MANE Select NP_000688.2:n.1161+101T>C