Canonical Allele Identifier: CA624868222

Gene: ALOX12B

Linked Data

• dbSNP Id: rs1430961639
• gnomAD v2: 17-7979960-G-A
• gnomAD v4: 17-8076642-G-A
• MyVariant Identifiers: chr17:g.7979960G>A (hg19) ; chr17:g.8076642G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8076642G>A , CM000679.2:g.8076642G>A	GRCh38
NC_000017.10:g.7979960G>A , CM000679.1:g.7979960G>A	GRCh37
NC_000017.9:g.7920685G>A	NCBI36
NG_007099.1:g.16062C>T
NG_007099.2:g.16075C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1362+15C>T MANE Select	ENSP00000497784.1:n.1362+15C>T
ENST00000649809.1:c.426+15C>T	ENSP00000496845.1:n.426+15C>T
ENST00000319144.4:c.1362+15C>T	ENSP00000315167.4:n.1362+15C>T
ENST00000577351.5:n.309+15C>T
ENST00000583276.5:n.746+15C>T
ENST00000584116.1:n.618+15C>T
NM_001139.2:c.1362+15C>T	NP_001130.1:n.1362+15C>T
NM_001139.3:c.1362+15C>T MANE Select	NP_001130.1:n.1362+15C>T