Canonical Allele Identifier: CA8367707
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs774907536
ExAC: 17:7989332 ACCTGTGGCCTC / A
gnomAD v2: 17-7989332-ACCTGTGGCCTC-A
gnomAD v4: 17-8086014-ACCTGTGGCCTC-A
MyVariant Identifiers: chr17:g.7989333_7989343del (hg19) chr17:g.8086015_8086025del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086017_8086027del , CM000679.2:g.8086017_8086027del GRCh38
NC_000017.10:g.7989335_7989345del , CM000679.1:g.7989335_7989345del GRCh37
NC_000017.9:g.7930060_7930070del NCBI36
NG_007099.1:g.6679_6689del
NG_007099.2:g.6692_6702del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.343_352+1del
ENST00000319144.4:c.343_352+1del
NM_001139.2:c.343_352+1del
NM_001139.3:c.343_352+1del
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