Canonical Allele Identifier: CA397737350
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1477355522
gnomAD v4: 17-6996851-C-T
MyVariant Identifiers: chr17:g.6900170C>T (hg19) chr17:g.6996851C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996851C>T , CM000679.2:g.6996851C>T GRCh38
NC_000017.10:g.6900170C>T , CM000679.1:g.6900170C>T GRCh37
NC_000017.9:g.6840894C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.161C>T (ALOX12) MANE Select ENSP00000251535.6:p.Ala54Val
ENST00000251535.10:c.161C>T (ALOX12) ENSP00000251535.6:p.Ala54Val
NM_000697.2:c.161C>T (ALOX12) NP_000688.2:p.Ala54Val
NR_040089.1:n.234-11311G>A (ALOX12-AS1)
XM_011523780.1:c.518C>T (ALOX12) XP_011522082.1:p.Ala173Val
XM_011523780.2:c.518C>T (ALOX12) XP_011522082.1:p.Ala173Val
NM_000697.3:c.161C>T (ALOX12) MANE Select NP_000688.2:p.Ala54Val
Search 100 bp 5'
Search 100 bp 3'