Canonical Allele Identifier: CA497759417

Gene: ALOX12B

Linked Data

• MyVariant Identifiers: chr17:g.7979639G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8076321G>T , CM000679.2:g.8076321G>T	GRCh38
NC_000017.10:g.7979639G>T , CM000679.1:g.7979639G>T	GRCh37
NC_000017.9:g.7920364G>T	NCBI36
NG_007099.1:g.16383C>A
NG_007099.2:g.16396C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1386C>A MANE Select	ENSP00000497784.1:p.Gly462=
ENST00000649809.1:c.450C>A	ENSP00000496845.1:p.Gly150=
ENST00000319144.4:c.1386C>A	ENSP00000315167.4:p.Gly462=
ENST00000577351.5:n.333C>A
ENST00000583276.5:n.770C>A
ENST00000584116.1:n.642C>A
NM_001139.2:c.1386C>A	NP_001130.1:p.Gly462=
NM_001139.3:c.1386C>A MANE Select	NP_001130.1:p.Gly462=