Canonical Allele Identifier: CA775590087
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs1377238836
gnomAD v3: 17-8085734-CG-C
gnomAD v4: 17-8085734-CG-C
MyVariant Identifiers: chr17:g.7989053del (hg19) chr17:g.8085735del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8085738del , CM000679.2:g.8085738del GRCh38
NC_000017.10:g.7989056del , CM000679.1:g.7989056del GRCh37
NC_000017.9:g.7929781del NCBI36
NG_007099.1:g.6969del
NG_007099.2:g.6982del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.352+281del MANE Select ENSP00000497784.1:n.352+281del
ENST00000319144.4:c.352+281del ENSP00000315167.4:n.352+281del
NM_001139.2:c.352+281del NP_001130.1:n.352+281del
NM_001139.3:c.352+281del MANE Select NP_001130.1:n.352+281del
Search 100 bp 5'
Search 100 bp 3'