Canonical Allele Identifier: CA2635745986
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-6996689-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996689G>A , CM000679.2:g.6996689G>A GRCh38
NC_000017.10:g.6900008G>A , CM000679.1:g.6900008G>A GRCh37
NC_000017.9:g.6840732G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000251535.11:c.136-137G>A (ALOX12) MANE Select ENSP00000251535.6:n.136-137G>A
ENST00000251535.10:c.136-137G>A (ALOX12) ENSP00000251535.6:n.136-137G>A
NM_000697.2:c.136-137G>A (ALOX12) NP_000688.2:n.136-137G>A
NR_040089.1:n.234-11149C>T (ALOX12-AS1)
XM_011523780.1:c.493-137G>A (ALOX12) XP_011522082.1:n.493-137G>A
XM_011523780.2:c.493-137G>A (ALOX12) XP_011522082.1:n.493-137G>A
NM_000697.3:c.136-137G>A (ALOX12) MANE Select NP_000688.2:n.136-137G>A