Canonical Allele Identifier: CA497598997
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1908464009
MyVariant Identifiers: chr17:g.6900168T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996849T>G , CM000679.2:g.6996849T>G GRCh38
NC_000017.10:g.6900168T>G , CM000679.1:g.6900168T>G GRCh37
NC_000017.9:g.6840892T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.159T>G (ALOX12) MANE Select ENSP00000251535.6:p.Val53=
ENST00000251535.10:c.159T>G (ALOX12) ENSP00000251535.6:p.Val53=
NM_000697.2:c.159T>G (ALOX12) NP_000688.2:p.Val53=
NR_040089.1:n.234-11309A>C (ALOX12-AS1)
XM_011523780.1:c.516T>G (ALOX12) XP_011522082.1:p.Val172=
XM_011523780.2:c.516T>G (ALOX12) XP_011522082.1:p.Val172=
NM_000697.3:c.159T>G (ALOX12) MANE Select NP_000688.2:p.Val53=
Search 100 bp 5'
Search 100 bp 3'