Canonical Allele Identifier: CA624860123
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1483735090
gnomAD v2: 17-6900390-C-A
gnomAD v4: 17-6997071-C-A
MyVariant Identifiers: chr17:g.6900390C>A (hg19) chr17:g.6997071C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6997071C>A , CM000679.2:g.6997071C>A GRCh38
NC_000017.10:g.6900390C>A , CM000679.1:g.6900390C>A GRCh37
NC_000017.9:g.6841114C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.337+44C>A (ALOX12) MANE Select ENSP00000251535.6:n.337+44C>A
ENST00000251535.10:c.337+44C>A (ALOX12) ENSP00000251535.6:n.337+44C>A
ENST00000480801.1:c.46+44C>A (ALOX12) ENSP00000467033.1:n.46+44C>A
NM_000697.2:c.337+44C>A (ALOX12) NP_000688.2:n.337+44C>A
NR_040089.1:n.234-11531G>T (ALOX12-AS1)
XM_011523780.1:c.694+44C>A (ALOX12) XP_011522082.1:n.694+44C>A
XM_011523780.2:c.694+44C>A (ALOX12) XP_011522082.1:n.694+44C>A
NM_000697.3:c.337+44C>A (ALOX12) MANE Select NP_000688.2:n.337+44C>A
Search 100 bp 5'
Search 100 bp 3'