Canonical Allele Identifier: CA624868480

Gene: ALOX12B

Linked Data

• dbSNP Id: rs919590887
• gnomAD v2: 17-7989216-T-C
• gnomAD v3: 17-8085898-T-C
• gnomAD v4: 17-8085898-T-C
• MyVariant Identifiers: chr17:g.7989216T>C (hg19) ; chr17:g.8085898T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8085898T>C , CM000679.2:g.8085898T>C	GRCh38
NC_000017.10:g.7989216T>C , CM000679.1:g.7989216T>C	GRCh37
NC_000017.9:g.7929941T>C	NCBI36
NG_007099.1:g.6806A>G
NG_007099.2:g.6819A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.352+118A>G MANE Select	ENSP00000497784.1:n.352+118A>G
ENST00000319144.4:c.352+118A>G	ENSP00000315167.4:n.352+118A>G
NM_001139.2:c.352+118A>G	NP_001130.1:n.352+118A>G
NM_001139.3:c.352+118A>G MANE Select	NP_001130.1:n.352+118A>G