Canonical Allele Identifier: CA497759462

Gene: ALOX12B

Linked Data

• MyVariant Identifiers: chr17:g.7979651C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8076333C>T , CM000679.2:g.8076333C>T	GRCh38
NC_000017.10:g.7979651C>T , CM000679.1:g.7979651C>T	GRCh37
NC_000017.9:g.7920376C>T	NCBI36
NG_007099.1:g.16371G>A
NG_007099.2:g.16384G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1374G>A MANE Select	ENSP00000497784.1:p.Leu458=
ENST00000649809.1:c.438G>A	ENSP00000496845.1:p.Leu146=
ENST00000319144.4:c.1374G>A	ENSP00000315167.4:p.Leu458=
ENST00000577351.5:n.321G>A
ENST00000583276.5:n.758G>A
ENST00000584116.1:n.630G>A
NM_001139.2:c.1374G>A	NP_001130.1:p.Leu458=
NM_001139.3:c.1374G>A MANE Select	NP_001130.1:p.Leu458=