Canonical Allele Identifier: CA397737157
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1201400268
gnomAD v2: 17-6900147-G-C
gnomAD v3: 17-6996828-G-C
gnomAD v4: 17-6996828-G-C
MyVariant Identifiers: chr17:g.6900147G>C (hg19) chr17:g.6996828G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996828G>C , CM000679.2:g.6996828G>C GRCh38
NC_000017.10:g.6900147G>C , CM000679.1:g.6900147G>C GRCh37
NC_000017.9:g.6840871G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.138G>C (ALOX12) MANE Select ENSP00000251535.6:p.Glu46Asp
ENST00000251535.10:c.138G>C (ALOX12) ENSP00000251535.6:p.Glu46Asp
NM_000697.2:c.138G>C (ALOX12) NP_000688.2:p.Glu46Asp
NR_040089.1:n.234-11288C>G (ALOX12-AS1)
XM_011523780.1:c.495G>C (ALOX12) XP_011522082.1:p.Glu165Asp
XM_011523780.2:c.495G>C (ALOX12) XP_011522082.1:p.Glu165Asp
NM_000697.3:c.138G>C (ALOX12) MANE Select NP_000688.2:p.Glu46Asp
Search 100 bp 5'
Search 100 bp 3'