Canonical Allele Identifier: CA497757871

Gene: ALOX12B

Linked Data

• gnomAD v4: 17-8075617-G-A
• MyVariant Identifiers: chr17:g.7978935G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8075617G>A , CM000679.2:g.8075617G>A	GRCh38
NC_000017.10:g.7978935G>A , CM000679.1:g.7978935G>A	GRCh37
NC_000017.9:g.7919660G>A	NCBI36
NG_007099.1:g.17087C>T
NG_007099.2:g.17100C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647874.1:c.1632C>T MANE Select	ENSP00000497784.1:p.Cys544=
ENST00000649809.1:c.696C>T	ENSP00000496845.1:p.Cys232=
ENST00000319144.4:c.1632C>T	ENSP00000315167.4:p.Cys544=
ENST00000577351.5:n.479+558C>T
NM_001139.2:c.1632C>T	NP_001130.1:p.Cys544=
NM_001139.3:c.1632C>T MANE Select	NP_001130.1:p.Cys544=