Canonical Allele Identifier: CA8333131
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs750978849
ExAC: 17:6900133 C / T
gnomAD v2: 17-6900133-C-T
gnomAD v3: 17-6996814-C-T
gnomAD v4: 17-6996814-C-T
MyVariant Identifiers: chr17:g.6900133C>T (hg19) chr17:g.6996814C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996814C>T , CM000679.2:g.6996814C>T GRCh38
NC_000017.10:g.6900133C>T , CM000679.1:g.6900133C>T GRCh37
NC_000017.9:g.6840857C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.136-12C>T (ALOX12) MANE Select ENSP00000251535.6:n.136-12C>T
ENST00000251535.10:c.136-12C>T (ALOX12) ENSP00000251535.6:n.136-12C>T
NM_000697.2:c.136-12C>T (ALOX12) NP_000688.2:n.136-12C>T
NR_040089.1:n.234-11274G>A (ALOX12-AS1)
XM_011523780.1:c.493-12C>T (ALOX12) XP_011522082.1:n.493-12C>T
XM_011523780.2:c.493-12C>T (ALOX12) XP_011522082.1:n.493-12C>T
NM_000697.3:c.136-12C>T (ALOX12) MANE Select NP_000688.2:n.136-12C>T
Search 100 bp 5'
Search 100 bp 3'