Canonical Allele Identifier: CA2245576046
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1597321100

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001535T>G , CM000679.2:g.7001535T>G GRCh38
NC_000017.10:g.6904854T>G , CM000679.1:g.6904854T>G GRCh37
NC_000017.9:g.6845578T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.952-67T>G (ALOX12) MANE Select ENSP00000251535.6:n.952-67T>G
ENST00000251535.10:c.952-67T>G (ALOX12) ENSP00000251535.6:n.952-67T>G
NM_000697.2:c.952-67T>G (ALOX12) NP_000688.2:n.952-67T>G
NR_040089.1:n.233+8261A>C (ALOX12-AS1)
XM_011523780.1:c.1102-67T>G (ALOX12) XP_011522082.1:n.1102-67T>G
XM_011523780.2:c.1102-67T>G (ALOX12) XP_011522082.1:n.1102-67T>G
NM_000697.3:c.952-67T>G (ALOX12) MANE Select NP_000688.2:n.952-67T>G