Canonical Allele Identifier: CA397737803
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.6900262G>C (hg19) chr17:g.6996943G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996943G>C , CM000679.2:g.6996943G>C GRCh38
NC_000017.10:g.6900262G>C , CM000679.1:g.6900262G>C GRCh37
NC_000017.9:g.6840986G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.253G>C (ALOX12) MANE Select ENSP00000251535.6:p.Gly85Arg
ENST00000251535.10:c.253G>C (ALOX12) ENSP00000251535.6:p.Gly85Arg
NM_000697.2:c.253G>C (ALOX12) NP_000688.2:p.Gly85Arg
NR_040089.1:n.234-11403C>G (ALOX12-AS1)
XM_011523780.1:c.610G>C (ALOX12) XP_011522082.1:p.Gly204Arg
XM_011523780.2:c.610G>C (ALOX12) XP_011522082.1:p.Gly204Arg
NM_000697.3:c.253G>C (ALOX12) MANE Select NP_000688.2:p.Gly85Arg
Search 100 bp 5'
Search 100 bp 3'