Canonical Allele Identifier: CA2246104174
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs1978295347
gnomAD v4: 17-8085889-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8085892del , CM000679.2:g.8085892del GRCh38
NC_000017.10:g.7989210del , CM000679.1:g.7989210del GRCh37
NC_000017.9:g.7929935del NCBI36
NG_007099.1:g.6814del
NG_007099.2:g.6827del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.352+126del MANE Select ENSP00000497784.1:n.352+126del
ENST00000319144.4:c.352+126del ENSP00000315167.4:n.352+126del
NM_001139.2:c.352+126del NP_001130.1:n.352+126del
NM_001139.3:c.352+126del MANE Select NP_001130.1:n.352+126del
Search 100 bp 5'
Search 100 bp 3'