Canonical Allele Identifier: CA2635961534

Gene: ALOX12B

Linked Data

• gnomAD v4: 17-8085984-CCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8085985_8085986del , CM000679.2:g.8085985_8085986del	GRCh38
NC_000017.10:g.7989303_7989304del , CM000679.1:g.7989303_7989304del	GRCh37
NC_000017.9:g.7930028_7930029del	NCBI36
NG_007099.1:g.6718_6719del
NG_007099.2:g.6731_6732del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.352+30_352+31del MANE Select	ENSP00000497784.1:n.352+30_352+31del
ENST00000319144.4:c.352+30_352+31del	ENSP00000315167.4:n.352+30_352+31del
NM_001139.2:c.352+30_352+31del	NP_001130.1:n.352+30_352+31del
NM_001139.3:c.352+30_352+31del MANE Select	NP_001130.1:n.352+30_352+31del