Canonical Allele Identifier: CA497758023

Gene: ALOX12B

Linked Data

• MyVariant Identifiers: chr17:g.7978980A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8075662A>G , CM000679.2:g.8075662A>G	GRCh38
NC_000017.10:g.7978980A>G , CM000679.1:g.7978980A>G	GRCh37
NC_000017.9:g.7919705A>G	NCBI36
NG_007099.1:g.17042T>C
NG_007099.2:g.17055T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1587T>C MANE Select	ENSP00000497784.1:p.Gly529=
ENST00000649809.1:c.651T>C	ENSP00000496845.1:p.Gly217=
ENST00000319144.4:c.1587T>C	ENSP00000315167.4:p.Gly529=
ENST00000577351.5:n.479+513T>C
NM_001139.2:c.1587T>C	NP_001130.1:p.Gly529=
NM_001139.3:c.1587T>C MANE Select	NP_001130.1:p.Gly529=