Canonical Allele Identifier: CA397738177
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1266751266
gnomAD v2: 17-6900308-T-C
gnomAD v3: 17-6996989-T-C
gnomAD v4: 17-6996989-T-C
MyVariant Identifiers: chr17:g.6900308T>C (hg19) chr17:g.6996989T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996989T>C , CM000679.2:g.6996989T>C GRCh38
NC_000017.10:g.6900308T>C , CM000679.1:g.6900308T>C GRCh37
NC_000017.9:g.6841032T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.299T>C (ALOX12) MANE Select ENSP00000251535.6:p.Val100Ala
ENST00000251535.10:c.299T>C (ALOX12) ENSP00000251535.6:p.Val100Ala
ENST00000480801.1:c.8T>C (ALOX12) ENSP00000467033.1:p.Val3Ala
NM_000697.2:c.299T>C (ALOX12) NP_000688.2:p.Val100Ala
NR_040089.1:n.234-11449A>G (ALOX12-AS1)
XM_011523780.1:c.656T>C (ALOX12) XP_011522082.1:p.Val219Ala
XM_011523780.2:c.656T>C (ALOX12) XP_011522082.1:p.Val219Ala
NM_000697.3:c.299T>C (ALOX12) MANE Select NP_000688.2:p.Val100Ala
Search 100 bp 5'
Search 100 bp 3'