Canonical Allele Identifier: CA774565151
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1431830478
gnomAD v3: 17-6996626-C-A
gnomAD v4: 17-6996626-C-A
MyVariant Identifiers: chr17:g.6899945C>A (hg19) chr17:g.6996626C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996626C>A , CM000679.2:g.6996626C>A GRCh38
NC_000017.10:g.6899945C>A , CM000679.1:g.6899945C>A GRCh37
NC_000017.9:g.6840669C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.136-200C>A (ALOX12) MANE Select ENSP00000251535.6:n.136-200C>A
ENST00000251535.10:c.136-200C>A (ALOX12) ENSP00000251535.6:n.136-200C>A
NM_000697.2:c.136-200C>A (ALOX12) NP_000688.2:n.136-200C>A
NR_040089.1:n.234-11086G>T (ALOX12-AS1)
XM_011523780.1:c.493-200C>A (ALOX12) XP_011522082.1:n.493-200C>A
XM_011523780.2:c.493-200C>A (ALOX12) XP_011522082.1:n.493-200C>A
NM_000697.3:c.136-200C>A (ALOX12) MANE Select NP_000688.2:n.136-200C>A
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