Canonical Allele Identifier: CA397738017
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-6996972-C-A
MyVariant Identifiers: chr17:g.6900291C>A (hg19) chr17:g.6996972C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996972C>A , CM000679.2:g.6996972C>A GRCh38
NC_000017.10:g.6900291C>A , CM000679.1:g.6900291C>A GRCh37
NC_000017.9:g.6841015C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.282C>A (ALOX12) MANE Select ENSP00000251535.6:p.Phe94Leu
ENST00000251535.10:c.282C>A (ALOX12) ENSP00000251535.6:p.Phe94Leu
NM_000697.2:c.282C>A (ALOX12) NP_000688.2:p.Phe94Leu
NR_040089.1:n.234-11432G>T (ALOX12-AS1)
XM_011523780.1:c.639C>A (ALOX12) XP_011522082.1:p.Phe213Leu
XM_011523780.2:c.639C>A (ALOX12) XP_011522082.1:p.Phe213Leu
NM_000697.3:c.282C>A (ALOX12) MANE Select NP_000688.2:p.Phe94Leu
Search 100 bp 5'
Search 100 bp 3'