Canonical Allele Identifier: CA8333147
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs746121469
ExAC: 17:6900243 C / G
gnomAD v2: 17-6900243-C-G
gnomAD v3: 17-6996924-C-G
gnomAD v4: 17-6996924-C-G
MyVariant Identifiers: chr17:g.6900243C>G (hg19) chr17:g.6996924C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6996924C>G , CM000679.2:g.6996924C>G GRCh38
NC_000017.10:g.6900243C>G , CM000679.1:g.6900243C>G GRCh37
NC_000017.9:g.6840967C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.234C>G (ALOX12) MANE Select ENSP00000251535.6:p.Cys78Trp
ENST00000251535.10:c.234C>G (ALOX12) ENSP00000251535.6:p.Cys78Trp
NM_000697.2:c.234C>G (ALOX12) NP_000688.2:p.Cys78Trp
NR_040089.1:n.234-11384G>C (ALOX12-AS1)
XM_011523780.1:c.591C>G (ALOX12) XP_011522082.1:p.Cys197Trp
XM_011523780.2:c.591C>G (ALOX12) XP_011522082.1:p.Cys197Trp
NM_000697.3:c.234C>G (ALOX12) MANE Select NP_000688.2:p.Cys78Trp
Search 100 bp 5'
Search 100 bp 3'