Canonical Allele Identifier: CA774566910
Gene: ALOX12 HGNC NCBI
ALOX12-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1032127807
gnomAD v3: 17-7001914-G-T
gnomAD v4: 17-7001914-G-T
MyVariant Identifiers: chr17:g.6905233G>T (hg19) chr17:g.7001914G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7001914G>T , CM000679.2:g.7001914G>T GRCh38
NC_000017.10:g.6905233G>T , CM000679.1:g.6905233G>T GRCh37
NC_000017.9:g.6845957G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000251535.11:c.1161+103G>T (ALOX12) MANE Select ENSP00000251535.6:n.1161+103G>T
ENST00000251535.10:c.1161+103G>T (ALOX12) ENSP00000251535.6:n.1161+103G>T
NM_000697.2:c.1161+103G>T (ALOX12) NP_000688.2:n.1161+103G>T
NR_040089.1:n.233+7882C>A (ALOX12-AS1)
XM_011523780.1:c.1311+103G>T (ALOX12) XP_011522082.1:n.1311+103G>T
XM_011523780.2:c.1311+103G>T (ALOX12) XP_011522082.1:n.1311+103G>T
NM_000697.3:c.1161+103G>T (ALOX12) MANE Select NP_000688.2:n.1161+103G>T
Search 100 bp 5'
Search 100 bp 3'