Canonical Allele Identifier: CA2246103876

Gene: ALOX12B

Linked Data

• dbSNP Id: rs1978294772

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8085707_8085708del , CM000679.2:g.8085707_8085708del	GRCh38
NC_000017.10:g.7989025_7989026del , CM000679.1:g.7989025_7989026del	GRCh37
NC_000017.9:g.7929750_7929751del	NCBI36
NG_007099.1:g.6996_6997del
NG_007099.2:g.7009_7010del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.352+308_352+309del MANE Select	ENSP00000497784.1:n.352+308_352+309del
ENST00000319144.4:c.352+308_352+309del	ENSP00000315167.4:n.352+308_352+309del
NM_001139.2:c.352+308_352+309del	NP_001130.1:n.352+308_352+309del
NM_001139.3:c.352+308_352+309del MANE Select	NP_001130.1:n.352+308_352+309del