Canonical Allele Identifier: CA397737380
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

COSMIC: COSM2975936
MyVariant Identifiers: chr17:g.6900179T>C (hg19) chr17:g.6996860T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996860T>C , CM000679.2:g.6996860T>C GRCh38
NC_000017.10:g.6900179T>C , CM000679.1:g.6900179T>C GRCh37
NC_000017.9:g.6840903T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.170T>C (ALOX12) MANE Select ENSP00000251535.6:p.Leu57Ser
ENST00000251535.10:c.170T>C (ALOX12) ENSP00000251535.6:p.Leu57Ser
NM_000697.2:c.170T>C (ALOX12) NP_000688.2:p.Leu57Ser
NR_040089.1:n.234-11320A>G (ALOX12-AS1)
XM_011523780.1:c.527T>C (ALOX12) XP_011522082.1:p.Leu176Ser
XM_011523780.2:c.527T>C (ALOX12) XP_011522082.1:p.Leu176Ser
NM_000697.3:c.170T>C (ALOX12) MANE Select NP_000688.2:p.Leu57Ser
Search 100 bp 5'
Search 100 bp 3'