Canonical Allele Identifier: CA397999959
Gene: ALOX12B HGNC NCBI

Linked Data

dbSNP Id: rs1567985357
gnomAD v4: 17-8086177-A-G
MyVariant Identifiers: chr17:g.7989495A>G (hg19) chr17:g.8086177A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8086177A>G , CM000679.2:g.8086177A>G GRCh38
NC_000017.10:g.7989495A>G , CM000679.1:g.7989495A>G GRCh37
NC_000017.9:g.7930220A>G NCBI36
NG_007099.1:g.6527T>C
NG_007099.2:g.6540T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647874.1:c.191T>C MANE Select ENSP00000497784.1:p.Leu64Pro
ENST00000319144.4:c.191T>C ENSP00000315167.4:p.Leu64Pro
NM_001139.2:c.191T>C NP_001130.1:p.Leu64Pro
NM_001139.3:c.191T>C MANE Select NP_001130.1:p.Leu64Pro
Search 100 bp 5'
Search 100 bp 3'