Canonical Allele Identifier: CA2635961868

Gene: ALOX12B

Linked Data

• gnomAD v4: 17-8086153-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8086154del , CM000679.2:g.8086154del	GRCh38
NC_000017.10:g.7989472del , CM000679.1:g.7989472del	GRCh37
NC_000017.9:g.7930197del	NCBI36
NG_007099.1:g.6550del
NG_007099.2:g.6563del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.214del MANE Select	ENSP00000497784.1:p.Glu72SerfsTer?
ENST00000319144.4:c.214del	ENSP00000315167.4:p.Glu72SerfsTer?
NM_001139.2:c.214del	NP_001130.1:p.Glu72SerfsTer?
NM_001139.3:c.214del MANE Select	NP_001130.1:p.Glu72SerfsTer?