Canonical Allele Identifier: CA2635962182
Gene: ALOX12B HGNC NCBI

Linked Data

gnomAD v4: 17-8086289-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086289G>A , CM000679.2:g.8086289G>A GRCh38
NC_000017.10:g.7989607G>A , CM000679.1:g.7989607G>A GRCh37
NC_000017.9:g.7930332G>A NCBI36
NG_007099.1:g.6415C>T
NG_007099.2:g.6428C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.148-69C>T MANE Select ENSP00000497784.1:n.148-69C>T
ENST00000319144.4:c.148-69C>T ENSP00000315167.4:n.148-69C>T
NM_001139.2:c.148-69C>T NP_001130.1:n.148-69C>T
NM_001139.3:c.148-69C>T MANE Select NP_001130.1:n.148-69C>T
Search 100 bp 5'
Search 100 bp 3'