Canonical Allele Identifier: CA2635962224
Gene: ALOX12B HGNC NCBI

Linked Data

gnomAD v4: 17-8086310-T-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086310T>A , CM000679.2:g.8086310T>A GRCh38
NC_000017.10:g.7989628T>A , CM000679.1:g.7989628T>A GRCh37
NC_000017.9:g.7930353T>A NCBI36
NG_007099.1:g.6394A>T
NG_007099.2:g.6407A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.148-90A>T MANE Select ENSP00000497784.1:n.148-90A>T
ENST00000319144.4:c.148-90A>T ENSP00000315167.4:n.148-90A>T
NM_001139.2:c.148-90A>T NP_001130.1:n.148-90A>T
NM_001139.3:c.148-90A>T MANE Select NP_001130.1:n.148-90A>T
Search 100 bp 5'
Search 100 bp 3'