Canonical Allele Identifier: CA287552720
Gene: ALOX12B HGNC NCBI

Linked Data

ClinVar Variation Id: 1292216
ClinVar RCV Id: RCV001714333
dbSNP Id: rs146068538
gnomAD v2: 17-7989604-T-TC
gnomAD v3: 17-8086286-T-TC
gnomAD v4: 17-8086286-T-TC
MyVariant Identifiers: chr17:g.7989604_7989605insC (hg19) chr17:g.8086286_8086287insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086287dup , CM000679.2:g.8086287dup GRCh38
NC_000017.10:g.7989605dup , CM000679.1:g.7989605dup GRCh37
NC_000017.9:g.7930330dup NCBI36
NG_007099.1:g.6417dup
NG_007099.2:g.6430dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.148-67dup MANE Select ENSP00000497784.1:n.148-67dup
ENST00000319144.4:c.148-67dup ENSP00000315167.4:n.148-67dup
NM_001139.2:c.148-67dup NP_001130.1:n.148-67dup
NM_001139.3:c.148-67dup MANE Select NP_001130.1:n.148-67dup
Search 100 bp 5'
Search 100 bp 3'