Canonical Allele Identifier: CA2635746183
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-6997085-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6997085G>A , CM000679.2:g.6997085G>A GRCh38
NC_000017.10:g.6900404G>A , CM000679.1:g.6900404G>A GRCh37
NC_000017.9:g.6841128G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.337+58G>A (ALOX12) MANE Select ENSP00000251535.6:n.337+58G>A
ENST00000251535.10:c.337+58G>A (ALOX12) ENSP00000251535.6:n.337+58G>A
ENST00000480801.1:c.46+58G>A (ALOX12) ENSP00000467033.1:n.46+58G>A
NM_000697.2:c.337+58G>A (ALOX12) NP_000688.2:n.337+58G>A
NR_040089.1:n.234-11545C>T (ALOX12-AS1)
XM_011523780.1:c.694+58G>A (ALOX12) XP_011522082.1:n.694+58G>A
XM_011523780.2:c.694+58G>A (ALOX12) XP_011522082.1:n.694+58G>A
NM_000697.3:c.337+58G>A (ALOX12) MANE Select NP_000688.2:n.337+58G>A