Canonical Allele Identifier: CA2635959551

Gene: ALOX12B

Linked Data

• gnomAD v4: 17-8076537-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8076537T>A , CM000679.2:g.8076537T>A	GRCh38
NC_000017.10:g.7979855T>A , CM000679.1:g.7979855T>A	GRCh37
NC_000017.9:g.7920580T>A	NCBI36
NG_007099.1:g.16167A>T
NG_007099.2:g.16180A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1362+120A>T MANE Select	ENSP00000497784.1:n.1362+120A>T
ENST00000649809.1:c.426+120A>T	ENSP00000496845.1:n.426+120A>T
ENST00000319144.4:c.1362+120A>T	ENSP00000315167.4:n.1362+120A>T
ENST00000577351.5:n.309+120A>T
ENST00000583276.5:n.746+120A>T
ENST00000584116.1:n.618+120A>T
NM_001139.2:c.1362+120A>T	NP_001130.1:n.1362+120A>T
NM_001139.3:c.1362+120A>T MANE Select	NP_001130.1:n.1362+120A>T