Canonical Allele Identifier: CA8333153
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs369870849
ExAC: 17:6900297 C / T
gnomAD v2: 17-6900297-C-T
gnomAD v3: 17-6996978-C-T
gnomAD v4: 17-6996978-C-T
MyVariant Identifiers: chr17:g.6900297C>T (hg19) chr17:g.6996978C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996978C>T , CM000679.2:g.6996978C>T GRCh38
NC_000017.10:g.6900297C>T , CM000679.1:g.6900297C>T GRCh37
NC_000017.9:g.6841021C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.288C>T (ALOX12) MANE Select ENSP00000251535.6:p.Cys96=
ENST00000251535.10:c.288C>T (ALOX12) ENSP00000251535.6:p.Cys96=
NM_000697.2:c.288C>T (ALOX12) NP_000688.2:p.Cys96=
NR_040089.1:n.234-11438G>A (ALOX12-AS1)
XM_011523780.1:c.645C>T (ALOX12) XP_011522082.1:p.Cys215=
XM_011523780.2:c.645C>T (ALOX12) XP_011522082.1:p.Cys215=
NM_000697.3:c.288C>T (ALOX12) MANE Select NP_000688.2:p.Cys96=
Search 100 bp 5'
Search 100 bp 3'