Canonical Allele Identifier: CA2635745980
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-6996684-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996684A>G , CM000679.2:g.6996684A>G GRCh38
NC_000017.10:g.6900003A>G , CM000679.1:g.6900003A>G GRCh37
NC_000017.9:g.6840727A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000251535.11:c.136-142A>G (ALOX12) MANE Select ENSP00000251535.6:n.136-142A>G
ENST00000251535.10:c.136-142A>G (ALOX12) ENSP00000251535.6:n.136-142A>G
NM_000697.2:c.136-142A>G (ALOX12) NP_000688.2:n.136-142A>G
NR_040089.1:n.234-11144T>C (ALOX12-AS1)
XM_011523780.1:c.493-142A>G (ALOX12) XP_011522082.1:n.493-142A>G
XM_011523780.2:c.493-142A>G (ALOX12) XP_011522082.1:n.493-142A>G
NM_000697.3:c.136-142A>G (ALOX12) MANE Select NP_000688.2:n.136-142A>G