Canonical Allele Identifier: CA2635962130

Gene: ALOX12B

Linked Data

• gnomAD v4: 17-8086273-GGCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8086277_8086279del , CM000679.2:g.8086277_8086279del	GRCh38
NC_000017.10:g.7989595_7989597del , CM000679.1:g.7989595_7989597del	GRCh37
NC_000017.9:g.7930320_7930322del	NCBI36
NG_007099.1:g.6428_6430del
NG_007099.2:g.6441_6443del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.148-56_148-54del MANE Select	ENSP00000497784.1:n.148-56_148-54del
ENST00000319144.4:c.148-56_148-54del	ENSP00000315167.4:n.148-56_148-54del
NM_001139.2:c.148-56_148-54del	NP_001130.1:n.148-56_148-54del
NM_001139.3:c.148-56_148-54del MANE Select	NP_001130.1:n.148-56_148-54del