Canonical Allele Identifier: CA397737466
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

gnomAD v4: 17-6996877-G-A
MyVariant Identifiers: chr17:g.6900196G>A (hg19) chr17:g.6996877G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996877G>A , CM000679.2:g.6996877G>A GRCh38
NC_000017.10:g.6900196G>A , CM000679.1:g.6900196G>A GRCh37
NC_000017.9:g.6840920G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.187G>A (ALOX12) MANE Select ENSP00000251535.6:p.Val63Met
ENST00000251535.10:c.187G>A (ALOX12) ENSP00000251535.6:p.Val63Met
NM_000697.2:c.187G>A (ALOX12) NP_000688.2:p.Val63Met
NR_040089.1:n.234-11337C>T (ALOX12-AS1)
XM_011523780.1:c.544G>A (ALOX12) XP_011522082.1:p.Val182Met
XM_011523780.2:c.544G>A (ALOX12) XP_011522082.1:p.Val182Met
NM_000697.3:c.187G>A (ALOX12) MANE Select NP_000688.2:p.Val63Met
Search 100 bp 5'
Search 100 bp 3'