Canonical Allele Identifier: CA2635961533

Gene: ALOX12B

Linked Data

• gnomAD v4: 17-8085981-CGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8085982_8085983del , CM000679.2:g.8085982_8085983del	GRCh38
NC_000017.10:g.7989300_7989301del , CM000679.1:g.7989300_7989301del	GRCh37
NC_000017.9:g.7930025_7930026del	NCBI36
NG_007099.1:g.6721_6722del
NG_007099.2:g.6734_6735del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.352+33_352+34del MANE Select	ENSP00000497784.1:n.352+33_352+34del
ENST00000319144.4:c.352+33_352+34del	ENSP00000315167.4:n.352+33_352+34del
NM_001139.2:c.352+33_352+34del	NP_001130.1:n.352+33_352+34del
NM_001139.3:c.352+33_352+34del MANE Select	NP_001130.1:n.352+33_352+34del