Canonical Allele Identifier: CA774565190
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1266105185
gnomAD v3: 17-6996767-T-C
gnomAD v4: 17-6996767-T-C
MyVariant Identifiers: chr17:g.6900086T>C (hg19) chr17:g.6996767T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996767T>C , CM000679.2:g.6996767T>C GRCh38
NC_000017.10:g.6900086T>C , CM000679.1:g.6900086T>C GRCh37
NC_000017.9:g.6840810T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000251535.11:c.136-59T>C (ALOX12) MANE Select ENSP00000251535.6:n.136-59T>C
ENST00000251535.10:c.136-59T>C (ALOX12) ENSP00000251535.6:n.136-59T>C
NM_000697.2:c.136-59T>C (ALOX12) NP_000688.2:n.136-59T>C
NR_040089.1:n.234-11227A>G (ALOX12-AS1)
XM_011523780.1:c.493-59T>C (ALOX12) XP_011522082.1:n.493-59T>C
XM_011523780.2:c.493-59T>C (ALOX12) XP_011522082.1:n.493-59T>C
NM_000697.3:c.136-59T>C (ALOX12) MANE Select NP_000688.2:n.136-59T>C
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