Canonical Allele Identifier: CA397738233
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-6996995-G-C
MyVariant Identifiers: chr17:g.6900314G>C (hg19) chr17:g.6996995G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996995G>C , CM000679.2:g.6996995G>C GRCh38
NC_000017.10:g.6900314G>C , CM000679.1:g.6900314G>C GRCh37
NC_000017.9:g.6841038G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.305G>C (ALOX12) MANE Select ENSP00000251535.6:p.Gly102Ala
ENST00000251535.10:c.305G>C (ALOX12) ENSP00000251535.6:p.Gly102Ala
ENST00000480801.1:c.14G>C (ALOX12) ENSP00000467033.1:p.Gly5Ala
NM_000697.2:c.305G>C (ALOX12) NP_000688.2:p.Gly102Ala
NR_040089.1:n.234-11455C>G (ALOX12-AS1)
XM_011523780.1:c.662G>C (ALOX12) XP_011522082.1:p.Gly221Ala
XM_011523780.2:c.662G>C (ALOX12) XP_011522082.1:p.Gly221Ala
NM_000697.3:c.305G>C (ALOX12) MANE Select NP_000688.2:p.Gly102Ala
Search 100 bp 5'
Search 100 bp 3'